Canonical Allele Identifier: CA1230390624

Gene: SDCCAG8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426537T= , CM000663.2:g.243426537T=	GRCh38
NC_000001.10:g.243589839T= , CM000663.1:g.243589839T=	GRCh37
NC_000001.9:g.241656462T=	NCBI36
NG_027811.1:g.175533T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1964T= MANE Select	ENSP00000355499.3:p.Val655=
ENST00000366541.7:c.1964T=	ENSP00000355499.3:p.Val655=
ENST00000435549.1:c.1067T=	ENSP00000410200.1:p.Val356=
ENST00000463042.1:n.171T=
NM_006642.3:c.1964T=	NP_006633.1:p.Val655=
XM_005273013.3:c.1835T=	XP_005273070.1:p.Val612=
XM_005273018.1:c.1541T=	XP_005273075.1:p.Val514=
XM_005273021.3:c.1061T=	XP_005273078.1:p.Val354=
XM_005273022.2:c.1043T=	XP_005273079.1:p.Val348=
XM_006711727.2:c.1994T=	XP_006711790.1:p.Val665=
XM_006711728.2:c.1865T=	XP_006711791.1:p.Val622=
XM_006711729.2:c.1805T=	XP_006711792.1:p.Val602=
XM_011544021.1:c.2090T=	XP_011542323.1:p.Val697=
XM_011544022.1:c.2060T=	XP_011542324.1:p.Val687=
XM_011544023.1:c.2090T=	XP_011542325.1:p.Val697=
XM_011544024.1:c.2090T=	XP_011542326.1:p.Val697=
XM_011544025.1:c.1901T=	XP_011542327.1:p.Val634=
XM_011544026.1:c.1853T=	XP_011542328.1:p.Val618=
XM_011544027.1:c.1676T=	XP_011542329.1:p.Val559=
XM_011544028.1:c.1628T=	XP_011542330.1:p.Val543=
XM_011544030.1:c.1019T=	XP_011542332.1:p.Val340=
XR_949128.1:n.2114T=
NM_001350246.1:c.1061T=	NP_001337175.1:p.Val354=
NM_001350247.1:c.1061T=	NP_001337176.1:p.Val354=
NM_001350248.1:c.2060T=	NP_001337177.1:p.Val687=
NM_001350249.1:c.1670T=	NP_001337178.1:p.Val557=
NM_001350251.1:c.1061T=	NP_001337180.1:p.Val354=
NM_006642.4:c.1964T=	NP_006633.1:p.Val655=
XM_005273013.5:c.1835T=	XP_005273070.1:p.Val612=
XM_005273018.2:c.1541T=	XP_005273075.1:p.Val514=
XM_005273022.4:c.1043T=	XP_005273079.1:p.Val348=
XM_011544026.3:c.1853T=	XP_011542328.1:p.Val618=
XM_011544028.3:c.1628T=	XP_011542330.1:p.Val543=
XM_011544030.3:c.1019T=	XP_011542332.1:p.Val340=
XM_017000104.2:c.1835T=	XP_016855593.1:p.Val612=
XM_017000105.2:c.1727T=	XP_016855594.1:p.Val576=
XM_024452537.1:c.1766T=	XP_024308305.1:p.Val589=
XM_024452539.1:c.1766T=	XP_024308307.1:p.Val589=
XM_024452540.1:c.1766T=	XP_024308308.1:p.Val589=
XM_024452547.1:c.1670T=	XP_024308315.1:p.Val557=
XM_024452548.1:c.1766T=	XP_024308316.1:p.Val589=
XM_024452549.1:c.1433T=	XP_024308317.1:p.Val478=
XR_002958955.1:n.2006T=
XR_002958956.1:n.2006T=
XR_002958965.1:n.1897T=
NM_006642.5:c.1964T= MANE Select	NP_006633.1:p.Val655=
NM_001350246.2:c.1061T=	NP_001337175.1:p.Val354=
NM_001350247.2:c.1061T=	NP_001337176.1:p.Val354=
NM_001350248.2:c.2060T=	NP_001337177.1:p.Val687=
NM_001350249.2:c.1670T=	NP_001337178.1:p.Val557=
NM_001350251.2:c.1061T=	NP_001337180.1:p.Val354=