Canonical Allele Identifier: CA345667646

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589734A>C (hg19) ; chr1:g.243426432A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426432A>C , CM000663.2:g.243426432A>C	GRCh38
NC_000001.10:g.243589734A>C , CM000663.1:g.243589734A>C	GRCh37
NC_000001.9:g.241656357A>C	NCBI36
NG_027811.1:g.175428A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1859A>C MANE Select	ENSP00000355499.3:p.Glu620Ala
ENST00000366541.7:c.1859A>C	ENSP00000355499.3:p.Glu620Ala
ENST00000435549.1:c.962A>C	ENSP00000410200.1:p.Glu321Ala
ENST00000463042.1:n.66A>C
NM_006642.3:c.1859A>C	NP_006633.1:p.Glu620Ala
XM_005273013.3:c.1730A>C	XP_005273070.1:p.Glu577Ala
XM_005273018.1:c.1436A>C	XP_005273075.1:p.Glu479Ala
XM_005273021.3:c.956A>C	XP_005273078.1:p.Glu319Ala
XM_005273022.2:c.938A>C	XP_005273079.1:p.Glu313Ala
XM_006711727.2:c.1889A>C	XP_006711790.1:p.Glu630Ala
XM_006711728.2:c.1760A>C	XP_006711791.1:p.Glu587Ala
XM_006711729.2:c.1700A>C	XP_006711792.1:p.Glu567Ala
XM_011544021.1:c.1985A>C	XP_011542323.1:p.Glu662Ala
XM_011544022.1:c.1955A>C	XP_011542324.1:p.Glu652Ala
XM_011544023.1:c.1985A>C	XP_011542325.1:p.Glu662Ala
XM_011544024.1:c.1985A>C	XP_011542326.1:p.Glu662Ala
XM_011544025.1:c.1796A>C	XP_011542327.1:p.Glu599Ala
XM_011544026.1:c.1748A>C	XP_011542328.1:p.Glu583Ala
XM_011544027.1:c.1571A>C	XP_011542329.1:p.Glu524Ala
XM_011544028.1:c.1523A>C	XP_011542330.1:p.Glu508Ala
XM_011544030.1:c.914A>C	XP_011542332.1:p.Glu305Ala
XR_949128.1:n.2009A>C
NM_001350246.1:c.956A>C	NP_001337175.1:p.Glu319Ala
NM_001350247.1:c.956A>C	NP_001337176.1:p.Glu319Ala
NM_001350248.1:c.1955A>C	NP_001337177.1:p.Glu652Ala
NM_001350249.1:c.1565A>C	NP_001337178.1:p.Glu522Ala
NM_001350251.1:c.956A>C	NP_001337180.1:p.Glu319Ala
NM_006642.4:c.1859A>C	NP_006633.1:p.Glu620Ala
XM_005273013.5:c.1730A>C	XP_005273070.1:p.Glu577Ala
XM_005273018.2:c.1436A>C	XP_005273075.1:p.Glu479Ala
XM_005273022.4:c.938A>C	XP_005273079.1:p.Glu313Ala
XM_011544026.3:c.1748A>C	XP_011542328.1:p.Glu583Ala
XM_011544028.3:c.1523A>C	XP_011542330.1:p.Glu508Ala
XM_011544030.3:c.914A>C	XP_011542332.1:p.Glu305Ala
XM_017000104.2:c.1730A>C	XP_016855593.1:p.Glu577Ala
XM_017000105.2:c.1622A>C	XP_016855594.1:p.Glu541Ala
XM_024452537.1:c.1661A>C	XP_024308305.1:p.Glu554Ala
XM_024452539.1:c.1661A>C	XP_024308307.1:p.Glu554Ala
XM_024452540.1:c.1661A>C	XP_024308308.1:p.Glu554Ala
XM_024452547.1:c.1565A>C	XP_024308315.1:p.Glu522Ala
XM_024452548.1:c.1661A>C	XP_024308316.1:p.Glu554Ala
XM_024452549.1:c.1328A>C	XP_024308317.1:p.Glu443Ala
XR_002958955.1:n.1901A>C
XR_002958956.1:n.1901A>C
XR_002958965.1:n.1792A>C
NM_006642.5:c.1859A>C MANE Select	NP_006633.1:p.Glu620Ala
NM_001350246.2:c.956A>C	NP_001337175.1:p.Glu319Ala
NM_001350247.2:c.956A>C	NP_001337176.1:p.Glu319Ala
NM_001350248.2:c.1955A>C	NP_001337177.1:p.Glu652Ala
NM_001350249.2:c.1565A>C	NP_001337178.1:p.Glu522Ala
NM_001350251.2:c.956A>C	NP_001337180.1:p.Glu319Ala