Canonical Allele Identifier: CA2748417858

Gene: SDCCAG8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426748_243426754del , CM000663.2:g.243426748_243426754del	GRCh38
NC_000001.10:g.243590050_243590056del , CM000663.1:g.243590050_243590056del	GRCh37
NC_000001.9:g.241656673_241656679del	NCBI36
NG_027811.1:g.175744_175750del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1985+190_1985+196del MANE Select	ENSP00000355499.3:n.1985+190_1985+196del
ENST00000366541.7:c.1985+190_1985+196del	ENSP00000355499.3:n.1985+190_1985+196del
ENST00000435549.1:c.1088+190_1088+196del	ENSP00000410200.1:n.1088+190_1088+196del
ENST00000463042.1:n.192+190_192+196del
NM_006642.3:c.1985+190_1985+196del	NP_006633.1:n.1985+190_1985+196del
XM_005273013.3:c.1856+190_1856+196del	XP_005273070.1:n.1856+190_1856+196del
XM_005273018.1:c.1562+190_1562+196del	XP_005273075.1:n.1562+190_1562+196del
XM_005273021.3:c.1082+190_1082+196del	XP_005273078.1:n.1082+190_1082+196del
XM_005273022.2:c.1064+190_1064+196del	XP_005273079.1:n.1064+190_1064+196del
XM_006711727.2:c.2015+190_2015+196del	XP_006711790.1:n.2015+190_2015+196del
XM_006711728.2:c.1886+190_1886+196del	XP_006711791.1:n.1886+190_1886+196del
XM_006711729.2:c.1826+190_1826+196del	XP_006711792.1:n.1826+190_1826+196del
XM_011544021.1:c.2111+190_2111+196del	XP_011542323.1:n.2111+190_2111+196del
XM_011544022.1:c.2081+190_2081+196del	XP_011542324.1:n.2081+190_2081+196del
XM_011544023.1:c.2111+190_2111+196del	XP_011542325.1:n.2111+190_2111+196del
XM_011544024.1:c.2111+190_2111+196del	XP_011542326.1:n.2111+190_2111+196del
XM_011544025.1:c.1922+190_1922+196del	XP_011542327.1:n.1922+190_1922+196del
XM_011544026.1:c.1874+190_1874+196del	XP_011542328.1:n.1874+190_1874+196del
XM_011544027.1:c.1697+190_1697+196del	XP_011542329.1:n.1697+190_1697+196del
XM_011544028.1:c.1649+190_1649+196del	XP_011542330.1:n.1649+190_1649+196del
XM_011544030.1:c.1040+190_1040+196del	XP_011542332.1:n.1040+190_1040+196del
XR_949128.1:n.2135+190_2135+196del
NM_001350246.1:c.1082+190_1082+196del	NP_001337175.1:n.1082+190_1082+196del
NM_001350247.1:c.1082+190_1082+196del	NP_001337176.1:n.1082+190_1082+196del
NM_001350248.1:c.2081+190_2081+196del	NP_001337177.1:n.2081+190_2081+196del
NM_001350249.1:c.1691+190_1691+196del	NP_001337178.1:n.1691+190_1691+196del
NM_001350251.1:c.1082+190_1082+196del	NP_001337180.1:n.1082+190_1082+196del
NM_006642.4:c.1985+190_1985+196del	NP_006633.1:n.1985+190_1985+196del
XM_005273013.5:c.1856+190_1856+196del	XP_005273070.1:n.1856+190_1856+196del
XM_005273018.2:c.1562+190_1562+196del	XP_005273075.1:n.1562+190_1562+196del
XM_005273022.4:c.1064+190_1064+196del	XP_005273079.1:n.1064+190_1064+196del
XM_011544026.3:c.1874+190_1874+196del	XP_011542328.1:n.1874+190_1874+196del
XM_011544028.3:c.1649+190_1649+196del	XP_011542330.1:n.1649+190_1649+196del
XM_011544030.3:c.1040+190_1040+196del	XP_011542332.1:n.1040+190_1040+196del
XM_017000104.2:c.1856+190_1856+196del	XP_016855593.1:n.1856+190_1856+196del
XM_017000105.2:c.1748+190_1748+196del	XP_016855594.1:n.1748+190_1748+196del
XM_024452537.1:c.1787+190_1787+196del	XP_024308305.1:n.1787+190_1787+196del
XM_024452539.1:c.1787+190_1787+196del	XP_024308307.1:n.1787+190_1787+196del
XM_024452540.1:c.1787+190_1787+196del	XP_024308308.1:n.1787+190_1787+196del
XM_024452547.1:c.1691+190_1691+196del	XP_024308315.1:n.1691+190_1691+196del
XM_024452548.1:c.1787+190_1787+196del	XP_024308316.1:n.1787+190_1787+196del
XM_024452549.1:c.1454+190_1454+196del	XP_024308317.1:n.1454+190_1454+196del
XR_002958955.1:n.2027+190_2027+196del
XR_002958956.1:n.2027+190_2027+196del
XR_002958965.1:n.1918+190_1918+196del
NM_006642.5:c.1985+190_1985+196del MANE Select	NP_006633.1:n.1985+190_1985+196del
NM_001350246.2:c.1082+190_1082+196del	NP_001337175.1:n.1082+190_1082+196del
NM_001350247.2:c.1082+190_1082+196del	NP_001337176.1:n.1082+190_1082+196del
NM_001350248.2:c.2081+190_2081+196del	NP_001337177.1:n.2081+190_2081+196del
NM_001350249.2:c.1691+190_1691+196del	NP_001337178.1:n.1691+190_1691+196del
NM_001350251.2:c.1082+190_1082+196del	NP_001337180.1:n.1082+190_1082+196del