Canonical Allele Identifier: CA345667682

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589750T>A (hg19) ; chr1:g.243426448T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426448T>A , CM000663.2:g.243426448T>A	GRCh38
NC_000001.10:g.243589750T>A , CM000663.1:g.243589750T>A	GRCh37
NC_000001.9:g.241656373T>A	NCBI36
NG_027811.1:g.175444T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1875T>A MANE Select	ENSP00000355499.3:p.Ser625Arg
ENST00000366541.7:c.1875T>A	ENSP00000355499.3:p.Ser625Arg
ENST00000435549.1:c.978T>A	ENSP00000410200.1:p.Ser326Arg
ENST00000463042.1:n.82T>A
NM_006642.3:c.1875T>A	NP_006633.1:p.Ser625Arg
XM_005273013.3:c.1746T>A	XP_005273070.1:p.Ser582Arg
XM_005273018.1:c.1452T>A	XP_005273075.1:p.Ser484Arg
XM_005273021.3:c.972T>A	XP_005273078.1:p.Ser324Arg
XM_005273022.2:c.954T>A	XP_005273079.1:p.Ser318Arg
XM_006711727.2:c.1905T>A	XP_006711790.1:p.Ser635Arg
XM_006711728.2:c.1776T>A	XP_006711791.1:p.Ser592Arg
XM_006711729.2:c.1716T>A	XP_006711792.1:p.Ser572Arg
XM_011544021.1:c.2001T>A	XP_011542323.1:p.Ser667Arg
XM_011544022.1:c.1971T>A	XP_011542324.1:p.Ser657Arg
XM_011544023.1:c.2001T>A	XP_011542325.1:p.Ser667Arg
XM_011544024.1:c.2001T>A	XP_011542326.1:p.Ser667Arg
XM_011544025.1:c.1812T>A	XP_011542327.1:p.Ser604Arg
XM_011544026.1:c.1764T>A	XP_011542328.1:p.Ser588Arg
XM_011544027.1:c.1587T>A	XP_011542329.1:p.Ser529Arg
XM_011544028.1:c.1539T>A	XP_011542330.1:p.Ser513Arg
XM_011544030.1:c.930T>A	XP_011542332.1:p.Ser310Arg
XR_949128.1:n.2025T>A
NM_001350246.1:c.972T>A	NP_001337175.1:p.Ser324Arg
NM_001350247.1:c.972T>A	NP_001337176.1:p.Ser324Arg
NM_001350248.1:c.1971T>A	NP_001337177.1:p.Ser657Arg
NM_001350249.1:c.1581T>A	NP_001337178.1:p.Ser527Arg
NM_001350251.1:c.972T>A	NP_001337180.1:p.Ser324Arg
NM_006642.4:c.1875T>A	NP_006633.1:p.Ser625Arg
XM_005273013.5:c.1746T>A	XP_005273070.1:p.Ser582Arg
XM_005273018.2:c.1452T>A	XP_005273075.1:p.Ser484Arg
XM_005273022.4:c.954T>A	XP_005273079.1:p.Ser318Arg
XM_011544026.3:c.1764T>A	XP_011542328.1:p.Ser588Arg
XM_011544028.3:c.1539T>A	XP_011542330.1:p.Ser513Arg
XM_011544030.3:c.930T>A	XP_011542332.1:p.Ser310Arg
XM_017000104.2:c.1746T>A	XP_016855593.1:p.Ser582Arg
XM_017000105.2:c.1638T>A	XP_016855594.1:p.Ser546Arg
XM_024452537.1:c.1677T>A	XP_024308305.1:p.Ser559Arg
XM_024452539.1:c.1677T>A	XP_024308307.1:p.Ser559Arg
XM_024452540.1:c.1677T>A	XP_024308308.1:p.Ser559Arg
XM_024452547.1:c.1581T>A	XP_024308315.1:p.Ser527Arg
XM_024452548.1:c.1677T>A	XP_024308316.1:p.Ser559Arg
XM_024452549.1:c.1344T>A	XP_024308317.1:p.Ser448Arg
XR_002958955.1:n.1917T>A
XR_002958956.1:n.1917T>A
XR_002958965.1:n.1808T>A
NM_006642.5:c.1875T>A MANE Select	NP_006633.1:p.Ser625Arg
NM_001350246.2:c.972T>A	NP_001337175.1:p.Ser324Arg
NM_001350247.2:c.972T>A	NP_001337176.1:p.Ser324Arg
NM_001350248.2:c.1971T>A	NP_001337177.1:p.Ser657Arg
NM_001350249.2:c.1581T>A	NP_001337178.1:p.Ser527Arg
NM_001350251.2:c.972T>A	NP_001337180.1:p.Ser324Arg