Canonical Allele Identifier: CA2748417855

Gene: SDCCAG8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426727_243426738del , CM000663.2:g.243426727_243426738del	GRCh38
NC_000001.10:g.243590029_243590040del , CM000663.1:g.243590029_243590040del	GRCh37
NC_000001.9:g.241656652_241656663del	NCBI36
NG_027811.1:g.175723_175734del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1985+169_1985+180del MANE Select	ENSP00000355499.3:n.1985+169_1985+180del
ENST00000366541.7:c.1985+169_1985+180del	ENSP00000355499.3:n.1985+169_1985+180del
ENST00000435549.1:c.1088+169_1088+180del	ENSP00000410200.1:n.1088+169_1088+180del
ENST00000463042.1:n.192+169_192+180del
NM_006642.3:c.1985+169_1985+180del	NP_006633.1:n.1985+169_1985+180del
XM_005273013.3:c.1856+169_1856+180del	XP_005273070.1:n.1856+169_1856+180del
XM_005273018.1:c.1562+169_1562+180del	XP_005273075.1:n.1562+169_1562+180del
XM_005273021.3:c.1082+169_1082+180del	XP_005273078.1:n.1082+169_1082+180del
XM_005273022.2:c.1064+169_1064+180del	XP_005273079.1:n.1064+169_1064+180del
XM_006711727.2:c.2015+169_2015+180del	XP_006711790.1:n.2015+169_2015+180del
XM_006711728.2:c.1886+169_1886+180del	XP_006711791.1:n.1886+169_1886+180del
XM_006711729.2:c.1826+169_1826+180del	XP_006711792.1:n.1826+169_1826+180del
XM_011544021.1:c.2111+169_2111+180del	XP_011542323.1:n.2111+169_2111+180del
XM_011544022.1:c.2081+169_2081+180del	XP_011542324.1:n.2081+169_2081+180del
XM_011544023.1:c.2111+169_2111+180del	XP_011542325.1:n.2111+169_2111+180del
XM_011544024.1:c.2111+169_2111+180del	XP_011542326.1:n.2111+169_2111+180del
XM_011544025.1:c.1922+169_1922+180del	XP_011542327.1:n.1922+169_1922+180del
XM_011544026.1:c.1874+169_1874+180del	XP_011542328.1:n.1874+169_1874+180del
XM_011544027.1:c.1697+169_1697+180del	XP_011542329.1:n.1697+169_1697+180del
XM_011544028.1:c.1649+169_1649+180del	XP_011542330.1:n.1649+169_1649+180del
XM_011544030.1:c.1040+169_1040+180del	XP_011542332.1:n.1040+169_1040+180del
XR_949128.1:n.2135+169_2135+180del
NM_001350246.1:c.1082+169_1082+180del	NP_001337175.1:n.1082+169_1082+180del
NM_001350247.1:c.1082+169_1082+180del	NP_001337176.1:n.1082+169_1082+180del
NM_001350248.1:c.2081+169_2081+180del	NP_001337177.1:n.2081+169_2081+180del
NM_001350249.1:c.1691+169_1691+180del	NP_001337178.1:n.1691+169_1691+180del
NM_001350251.1:c.1082+169_1082+180del	NP_001337180.1:n.1082+169_1082+180del
NM_006642.4:c.1985+169_1985+180del	NP_006633.1:n.1985+169_1985+180del
XM_005273013.5:c.1856+169_1856+180del	XP_005273070.1:n.1856+169_1856+180del
XM_005273018.2:c.1562+169_1562+180del	XP_005273075.1:n.1562+169_1562+180del
XM_005273022.4:c.1064+169_1064+180del	XP_005273079.1:n.1064+169_1064+180del
XM_011544026.3:c.1874+169_1874+180del	XP_011542328.1:n.1874+169_1874+180del
XM_011544028.3:c.1649+169_1649+180del	XP_011542330.1:n.1649+169_1649+180del
XM_011544030.3:c.1040+169_1040+180del	XP_011542332.1:n.1040+169_1040+180del
XM_017000104.2:c.1856+169_1856+180del	XP_016855593.1:n.1856+169_1856+180del
XM_017000105.2:c.1748+169_1748+180del	XP_016855594.1:n.1748+169_1748+180del
XM_024452537.1:c.1787+169_1787+180del	XP_024308305.1:n.1787+169_1787+180del
XM_024452539.1:c.1787+169_1787+180del	XP_024308307.1:n.1787+169_1787+180del
XM_024452540.1:c.1787+169_1787+180del	XP_024308308.1:n.1787+169_1787+180del
XM_024452547.1:c.1691+169_1691+180del	XP_024308315.1:n.1691+169_1691+180del
XM_024452548.1:c.1787+169_1787+180del	XP_024308316.1:n.1787+169_1787+180del
XM_024452549.1:c.1454+169_1454+180del	XP_024308317.1:n.1454+169_1454+180del
XR_002958955.1:n.2027+169_2027+180del
XR_002958956.1:n.2027+169_2027+180del
XR_002958965.1:n.1918+169_1918+180del
NM_006642.5:c.1985+169_1985+180del MANE Select	NP_006633.1:n.1985+169_1985+180del
NM_001350246.2:c.1082+169_1082+180del	NP_001337175.1:n.1082+169_1082+180del
NM_001350247.2:c.1082+169_1082+180del	NP_001337176.1:n.1082+169_1082+180del
NM_001350248.2:c.2081+169_2081+180del	NP_001337177.1:n.2081+169_2081+180del
NM_001350249.2:c.1691+169_1691+180del	NP_001337178.1:n.1691+169_1691+180del
NM_001350251.2:c.1082+169_1082+180del	NP_001337180.1:n.1082+169_1082+180del