Canonical Allele Identifier: CA345667649

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589735A>C (hg19) ; chr1:g.243426433A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426433A>C , CM000663.2:g.243426433A>C	GRCh38
NC_000001.10:g.243589735A>C , CM000663.1:g.243589735A>C	GRCh37
NC_000001.9:g.241656358A>C	NCBI36
NG_027811.1:g.175429A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1860A>C MANE Select	ENSP00000355499.3:p.Glu620Asp
ENST00000366541.7:c.1860A>C	ENSP00000355499.3:p.Glu620Asp
ENST00000435549.1:c.963A>C	ENSP00000410200.1:p.Glu321Asp
ENST00000463042.1:n.67A>C
NM_006642.3:c.1860A>C	NP_006633.1:p.Glu620Asp
XM_005273013.3:c.1731A>C	XP_005273070.1:p.Glu577Asp
XM_005273018.1:c.1437A>C	XP_005273075.1:p.Glu479Asp
XM_005273021.3:c.957A>C	XP_005273078.1:p.Glu319Asp
XM_005273022.2:c.939A>C	XP_005273079.1:p.Glu313Asp
XM_006711727.2:c.1890A>C	XP_006711790.1:p.Glu630Asp
XM_006711728.2:c.1761A>C	XP_006711791.1:p.Glu587Asp
XM_006711729.2:c.1701A>C	XP_006711792.1:p.Glu567Asp
XM_011544021.1:c.1986A>C	XP_011542323.1:p.Glu662Asp
XM_011544022.1:c.1956A>C	XP_011542324.1:p.Glu652Asp
XM_011544023.1:c.1986A>C	XP_011542325.1:p.Glu662Asp
XM_011544024.1:c.1986A>C	XP_011542326.1:p.Glu662Asp
XM_011544025.1:c.1797A>C	XP_011542327.1:p.Glu599Asp
XM_011544026.1:c.1749A>C	XP_011542328.1:p.Glu583Asp
XM_011544027.1:c.1572A>C	XP_011542329.1:p.Glu524Asp
XM_011544028.1:c.1524A>C	XP_011542330.1:p.Glu508Asp
XM_011544030.1:c.915A>C	XP_011542332.1:p.Glu305Asp
XR_949128.1:n.2010A>C
NM_001350246.1:c.957A>C	NP_001337175.1:p.Glu319Asp
NM_001350247.1:c.957A>C	NP_001337176.1:p.Glu319Asp
NM_001350248.1:c.1956A>C	NP_001337177.1:p.Glu652Asp
NM_001350249.1:c.1566A>C	NP_001337178.1:p.Glu522Asp
NM_001350251.1:c.957A>C	NP_001337180.1:p.Glu319Asp
NM_006642.4:c.1860A>C	NP_006633.1:p.Glu620Asp
XM_005273013.5:c.1731A>C	XP_005273070.1:p.Glu577Asp
XM_005273018.2:c.1437A>C	XP_005273075.1:p.Glu479Asp
XM_005273022.4:c.939A>C	XP_005273079.1:p.Glu313Asp
XM_011544026.3:c.1749A>C	XP_011542328.1:p.Glu583Asp
XM_011544028.3:c.1524A>C	XP_011542330.1:p.Glu508Asp
XM_011544030.3:c.915A>C	XP_011542332.1:p.Glu305Asp
XM_017000104.2:c.1731A>C	XP_016855593.1:p.Glu577Asp
XM_017000105.2:c.1623A>C	XP_016855594.1:p.Glu541Asp
XM_024452537.1:c.1662A>C	XP_024308305.1:p.Glu554Asp
XM_024452539.1:c.1662A>C	XP_024308307.1:p.Glu554Asp
XM_024452540.1:c.1662A>C	XP_024308308.1:p.Glu554Asp
XM_024452547.1:c.1566A>C	XP_024308315.1:p.Glu522Asp
XM_024452548.1:c.1662A>C	XP_024308316.1:p.Glu554Asp
XM_024452549.1:c.1329A>C	XP_024308317.1:p.Glu443Asp
XR_002958955.1:n.1902A>C
XR_002958956.1:n.1902A>C
XR_002958965.1:n.1793A>C
NM_006642.5:c.1860A>C MANE Select	NP_006633.1:p.Glu620Asp
NM_001350246.2:c.957A>C	NP_001337175.1:p.Glu319Asp
NM_001350247.2:c.957A>C	NP_001337176.1:p.Glu319Asp
NM_001350248.2:c.1956A>C	NP_001337177.1:p.Glu652Asp
NM_001350249.2:c.1566A>C	NP_001337178.1:p.Glu522Asp
NM_001350251.2:c.957A>C	NP_001337180.1:p.Glu319Asp