Canonical Allele Identifier: CA345667644

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589733G>C (hg19) ; chr1:g.243426431G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426431G>C , CM000663.2:g.243426431G>C	GRCh38
NC_000001.10:g.243589733G>C , CM000663.1:g.243589733G>C	GRCh37
NC_000001.9:g.241656356G>C	NCBI36
NG_027811.1:g.175427G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1858G>C MANE Select	ENSP00000355499.3:p.Glu620Gln
ENST00000366541.7:c.1858G>C	ENSP00000355499.3:p.Glu620Gln
ENST00000435549.1:c.961G>C	ENSP00000410200.1:p.Glu321Gln
ENST00000463042.1:n.65G>C
NM_006642.3:c.1858G>C	NP_006633.1:p.Glu620Gln
XM_005273013.3:c.1729G>C	XP_005273070.1:p.Glu577Gln
XM_005273018.1:c.1435G>C	XP_005273075.1:p.Glu479Gln
XM_005273021.3:c.955G>C	XP_005273078.1:p.Glu319Gln
XM_005273022.2:c.937G>C	XP_005273079.1:p.Glu313Gln
XM_006711727.2:c.1888G>C	XP_006711790.1:p.Glu630Gln
XM_006711728.2:c.1759G>C	XP_006711791.1:p.Glu587Gln
XM_006711729.2:c.1699G>C	XP_006711792.1:p.Glu567Gln
XM_011544021.1:c.1984G>C	XP_011542323.1:p.Glu662Gln
XM_011544022.1:c.1954G>C	XP_011542324.1:p.Glu652Gln
XM_011544023.1:c.1984G>C	XP_011542325.1:p.Glu662Gln
XM_011544024.1:c.1984G>C	XP_011542326.1:p.Glu662Gln
XM_011544025.1:c.1795G>C	XP_011542327.1:p.Glu599Gln
XM_011544026.1:c.1747G>C	XP_011542328.1:p.Glu583Gln
XM_011544027.1:c.1570G>C	XP_011542329.1:p.Glu524Gln
XM_011544028.1:c.1522G>C	XP_011542330.1:p.Glu508Gln
XM_011544030.1:c.913G>C	XP_011542332.1:p.Glu305Gln
XR_949128.1:n.2008G>C
NM_001350246.1:c.955G>C	NP_001337175.1:p.Glu319Gln
NM_001350247.1:c.955G>C	NP_001337176.1:p.Glu319Gln
NM_001350248.1:c.1954G>C	NP_001337177.1:p.Glu652Gln
NM_001350249.1:c.1564G>C	NP_001337178.1:p.Glu522Gln
NM_001350251.1:c.955G>C	NP_001337180.1:p.Glu319Gln
NM_006642.4:c.1858G>C	NP_006633.1:p.Glu620Gln
XM_005273013.5:c.1729G>C	XP_005273070.1:p.Glu577Gln
XM_005273018.2:c.1435G>C	XP_005273075.1:p.Glu479Gln
XM_005273022.4:c.937G>C	XP_005273079.1:p.Glu313Gln
XM_011544026.3:c.1747G>C	XP_011542328.1:p.Glu583Gln
XM_011544028.3:c.1522G>C	XP_011542330.1:p.Glu508Gln
XM_011544030.3:c.913G>C	XP_011542332.1:p.Glu305Gln
XM_017000104.2:c.1729G>C	XP_016855593.1:p.Glu577Gln
XM_017000105.2:c.1621G>C	XP_016855594.1:p.Glu541Gln
XM_024452537.1:c.1660G>C	XP_024308305.1:p.Glu554Gln
XM_024452539.1:c.1660G>C	XP_024308307.1:p.Glu554Gln
XM_024452540.1:c.1660G>C	XP_024308308.1:p.Glu554Gln
XM_024452547.1:c.1564G>C	XP_024308315.1:p.Glu522Gln
XM_024452548.1:c.1660G>C	XP_024308316.1:p.Glu554Gln
XM_024452549.1:c.1327G>C	XP_024308317.1:p.Glu443Gln
XR_002958955.1:n.1900G>C
XR_002958956.1:n.1900G>C
XR_002958965.1:n.1791G>C
NM_006642.5:c.1858G>C MANE Select	NP_006633.1:p.Glu620Gln
NM_001350246.2:c.955G>C	NP_001337175.1:p.Glu319Gln
NM_001350247.2:c.955G>C	NP_001337176.1:p.Glu319Gln
NM_001350248.2:c.1954G>C	NP_001337177.1:p.Glu652Gln
NM_001350249.2:c.1564G>C	NP_001337178.1:p.Glu522Gln
NM_001350251.2:c.955G>C	NP_001337180.1:p.Glu319Gln