Canonical Allele Identifier: CA424346888

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589834G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426532G>T , CM000663.2:g.243426532G>T	GRCh38
NC_000001.10:g.243589834G>T , CM000663.1:g.243589834G>T	GRCh37
NC_000001.9:g.241656457G>T	NCBI36
NG_027811.1:g.175528G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1959G>T MANE Select	ENSP00000355499.3:p.Gly653=
ENST00000366541.7:c.1959G>T	ENSP00000355499.3:p.Gly653=
ENST00000435549.1:c.1062G>T	ENSP00000410200.1:p.Gly354=
ENST00000463042.1:n.166G>T
NM_006642.3:c.1959G>T	NP_006633.1:p.Gly653=
XM_005273013.3:c.1830G>T	XP_005273070.1:p.Gly610=
XM_005273018.1:c.1536G>T	XP_005273075.1:p.Gly512=
XM_005273021.3:c.1056G>T	XP_005273078.1:p.Gly352=
XM_005273022.2:c.1038G>T	XP_005273079.1:p.Gly346=
XM_006711727.2:c.1989G>T	XP_006711790.1:p.Gly663=
XM_006711728.2:c.1860G>T	XP_006711791.1:p.Gly620=
XM_006711729.2:c.1800G>T	XP_006711792.1:p.Gly600=
XM_011544021.1:c.2085G>T	XP_011542323.1:p.Gly695=
XM_011544022.1:c.2055G>T	XP_011542324.1:p.Gly685=
XM_011544023.1:c.2085G>T	XP_011542325.1:p.Gly695=
XM_011544024.1:c.2085G>T	XP_011542326.1:p.Gly695=
XM_011544025.1:c.1896G>T	XP_011542327.1:p.Gly632=
XM_011544026.1:c.1848G>T	XP_011542328.1:p.Gly616=
XM_011544027.1:c.1671G>T	XP_011542329.1:p.Gly557=
XM_011544028.1:c.1623G>T	XP_011542330.1:p.Gly541=
XM_011544030.1:c.1014G>T	XP_011542332.1:p.Gly338=
XR_949128.1:n.2109G>T
NM_001350246.1:c.1056G>T	NP_001337175.1:p.Gly352=
NM_001350247.1:c.1056G>T	NP_001337176.1:p.Gly352=
NM_001350248.1:c.2055G>T	NP_001337177.1:p.Gly685=
NM_001350249.1:c.1665G>T	NP_001337178.1:p.Gly555=
NM_001350251.1:c.1056G>T	NP_001337180.1:p.Gly352=
NM_006642.4:c.1959G>T	NP_006633.1:p.Gly653=
XM_005273013.5:c.1830G>T	XP_005273070.1:p.Gly610=
XM_005273018.2:c.1536G>T	XP_005273075.1:p.Gly512=
XM_005273022.4:c.1038G>T	XP_005273079.1:p.Gly346=
XM_011544026.3:c.1848G>T	XP_011542328.1:p.Gly616=
XM_011544028.3:c.1623G>T	XP_011542330.1:p.Gly541=
XM_011544030.3:c.1014G>T	XP_011542332.1:p.Gly338=
XM_017000104.2:c.1830G>T	XP_016855593.1:p.Gly610=
XM_017000105.2:c.1722G>T	XP_016855594.1:p.Gly574=
XM_024452537.1:c.1761G>T	XP_024308305.1:p.Gly587=
XM_024452539.1:c.1761G>T	XP_024308307.1:p.Gly587=
XM_024452540.1:c.1761G>T	XP_024308308.1:p.Gly587=
XM_024452547.1:c.1665G>T	XP_024308315.1:p.Gly555=
XM_024452548.1:c.1761G>T	XP_024308316.1:p.Gly587=
XM_024452549.1:c.1428G>T	XP_024308317.1:p.Gly476=
XR_002958955.1:n.2001G>T
XR_002958956.1:n.2001G>T
XR_002958965.1:n.1892G>T
NM_006642.5:c.1959G>T MANE Select	NP_006633.1:p.Gly653=
NM_001350246.2:c.1056G>T	NP_001337175.1:p.Gly352=
NM_001350247.2:c.1056G>T	NP_001337176.1:p.Gly352=
NM_001350248.2:c.2055G>T	NP_001337177.1:p.Gly685=
NM_001350249.2:c.1665G>T	NP_001337178.1:p.Gly555=
NM_001350251.2:c.1056G>T	NP_001337180.1:p.Gly352=