Canonical Allele Identifier: CA1014176909
Gene: SDCCAG8 HGNC NCBI

Linked Data

dbSNP Id: rs2081369737

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.243426768_243426770del , CM000663.2:g.243426768_243426770del GRCh38
NC_000001.10:g.243590070_243590072del , CM000663.1:g.243590070_243590072del GRCh37
NC_000001.9:g.241656693_241656695del NCBI36
NG_027811.1:g.175764_175766del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366541.8:c.1985+210_1985+212del MANE Select ENSP00000355499.3:n.1985+210_1985+212del
ENST00000366541.7:c.1985+210_1985+212del ENSP00000355499.3:n.1985+210_1985+212del
ENST00000435549.1:c.1088+210_1088+212del ENSP00000410200.1:n.1088+210_1088+212del
ENST00000463042.1:n.192+210_192+212del
NM_006642.3:c.1985+210_1985+212del NP_006633.1:n.1985+210_1985+212del
XM_005273013.3:c.1856+210_1856+212del XP_005273070.1:n.1856+210_1856+212del
XM_005273018.1:c.1562+210_1562+212del XP_005273075.1:n.1562+210_1562+212del
XM_005273021.3:c.1082+210_1082+212del XP_005273078.1:n.1082+210_1082+212del
XM_005273022.2:c.1064+210_1064+212del XP_005273079.1:n.1064+210_1064+212del
XM_006711727.2:c.2015+210_2015+212del XP_006711790.1:n.2015+210_2015+212del
XM_006711728.2:c.1886+210_1886+212del XP_006711791.1:n.1886+210_1886+212del
XM_006711729.2:c.1826+210_1826+212del XP_006711792.1:n.1826+210_1826+212del
XM_011544021.1:c.2111+210_2111+212del XP_011542323.1:n.2111+210_2111+212del
XM_011544022.1:c.2081+210_2081+212del XP_011542324.1:n.2081+210_2081+212del
XM_011544023.1:c.2111+210_2111+212del XP_011542325.1:n.2111+210_2111+212del
XM_011544024.1:c.2111+210_2111+212del XP_011542326.1:n.2111+210_2111+212del
XM_011544025.1:c.1922+210_1922+212del XP_011542327.1:n.1922+210_1922+212del
XM_011544026.1:c.1874+210_1874+212del XP_011542328.1:n.1874+210_1874+212del
XM_011544027.1:c.1697+210_1697+212del XP_011542329.1:n.1697+210_1697+212del
XM_011544028.1:c.1649+210_1649+212del XP_011542330.1:n.1649+210_1649+212del
XM_011544030.1:c.1040+210_1040+212del XP_011542332.1:n.1040+210_1040+212del
XR_949128.1:n.2135+210_2135+212del
NM_001350246.1:c.1082+210_1082+212del NP_001337175.1:n.1082+210_1082+212del
NM_001350247.1:c.1082+210_1082+212del NP_001337176.1:n.1082+210_1082+212del
NM_001350248.1:c.2081+210_2081+212del NP_001337177.1:n.2081+210_2081+212del
NM_001350249.1:c.1691+210_1691+212del NP_001337178.1:n.1691+210_1691+212del
NM_001350251.1:c.1082+210_1082+212del NP_001337180.1:n.1082+210_1082+212del
NM_006642.4:c.1985+210_1985+212del NP_006633.1:n.1985+210_1985+212del
XM_005273013.5:c.1856+210_1856+212del XP_005273070.1:n.1856+210_1856+212del
XM_005273018.2:c.1562+210_1562+212del XP_005273075.1:n.1562+210_1562+212del
XM_005273022.4:c.1064+210_1064+212del XP_005273079.1:n.1064+210_1064+212del
XM_011544026.3:c.1874+210_1874+212del XP_011542328.1:n.1874+210_1874+212del
XM_011544028.3:c.1649+210_1649+212del XP_011542330.1:n.1649+210_1649+212del
XM_011544030.3:c.1040+210_1040+212del XP_011542332.1:n.1040+210_1040+212del
XM_017000104.2:c.1856+210_1856+212del XP_016855593.1:n.1856+210_1856+212del
XM_017000105.2:c.1748+210_1748+212del XP_016855594.1:n.1748+210_1748+212del
XM_024452537.1:c.1787+210_1787+212del XP_024308305.1:n.1787+210_1787+212del
XM_024452539.1:c.1787+210_1787+212del XP_024308307.1:n.1787+210_1787+212del
XM_024452540.1:c.1787+210_1787+212del XP_024308308.1:n.1787+210_1787+212del
XM_024452547.1:c.1691+210_1691+212del XP_024308315.1:n.1691+210_1691+212del
XM_024452548.1:c.1787+210_1787+212del XP_024308316.1:n.1787+210_1787+212del
XM_024452549.1:c.1454+210_1454+212del XP_024308317.1:n.1454+210_1454+212del
XR_002958955.1:n.2027+210_2027+212del
XR_002958956.1:n.2027+210_2027+212del
XR_002958965.1:n.1918+210_1918+212del
NM_006642.5:c.1985+210_1985+212del MANE Select NP_006633.1:n.1985+210_1985+212del
NM_001350246.2:c.1082+210_1082+212del NP_001337175.1:n.1082+210_1082+212del
NM_001350247.2:c.1082+210_1082+212del NP_001337176.1:n.1082+210_1082+212del
NM_001350248.2:c.2081+210_2081+212del NP_001337177.1:n.2081+210_2081+212del
NM_001350249.2:c.1691+210_1691+212del NP_001337178.1:n.1691+210_1691+212del
NM_001350251.2:c.1082+210_1082+212del NP_001337180.1:n.1082+210_1082+212del