Canonical Allele Identifier: CA345667841

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589818A>C (hg19) ; chr1:g.243426516A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426516A>C , CM000663.2:g.243426516A>C	GRCh38
NC_000001.10:g.243589818A>C , CM000663.1:g.243589818A>C	GRCh37
NC_000001.9:g.241656441A>C	NCBI36
NG_027811.1:g.175512A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1943A>C MANE Select	ENSP00000355499.3:p.Gln648Pro
ENST00000366541.7:c.1943A>C	ENSP00000355499.3:p.Gln648Pro
ENST00000435549.1:c.1046A>C	ENSP00000410200.1:p.Gln349Pro
ENST00000463042.1:n.150A>C
NM_006642.3:c.1943A>C	NP_006633.1:p.Gln648Pro
XM_005273013.3:c.1814A>C	XP_005273070.1:p.Gln605Pro
XM_005273018.1:c.1520A>C	XP_005273075.1:p.Gln507Pro
XM_005273021.3:c.1040A>C	XP_005273078.1:p.Gln347Pro
XM_005273022.2:c.1022A>C	XP_005273079.1:p.Gln341Pro
XM_006711727.2:c.1973A>C	XP_006711790.1:p.Gln658Pro
XM_006711728.2:c.1844A>C	XP_006711791.1:p.Gln615Pro
XM_006711729.2:c.1784A>C	XP_006711792.1:p.Gln595Pro
XM_011544021.1:c.2069A>C	XP_011542323.1:p.Gln690Pro
XM_011544022.1:c.2039A>C	XP_011542324.1:p.Gln680Pro
XM_011544023.1:c.2069A>C	XP_011542325.1:p.Gln690Pro
XM_011544024.1:c.2069A>C	XP_011542326.1:p.Gln690Pro
XM_011544025.1:c.1880A>C	XP_011542327.1:p.Gln627Pro
XM_011544026.1:c.1832A>C	XP_011542328.1:p.Gln611Pro
XM_011544027.1:c.1655A>C	XP_011542329.1:p.Gln552Pro
XM_011544028.1:c.1607A>C	XP_011542330.1:p.Gln536Pro
XM_011544030.1:c.998A>C	XP_011542332.1:p.Gln333Pro
XR_949128.1:n.2093A>C
NM_001350246.1:c.1040A>C	NP_001337175.1:p.Gln347Pro
NM_001350247.1:c.1040A>C	NP_001337176.1:p.Gln347Pro
NM_001350248.1:c.2039A>C	NP_001337177.1:p.Gln680Pro
NM_001350249.1:c.1649A>C	NP_001337178.1:p.Gln550Pro
NM_001350251.1:c.1040A>C	NP_001337180.1:p.Gln347Pro
NM_006642.4:c.1943A>C	NP_006633.1:p.Gln648Pro
XM_005273013.5:c.1814A>C	XP_005273070.1:p.Gln605Pro
XM_005273018.2:c.1520A>C	XP_005273075.1:p.Gln507Pro
XM_005273022.4:c.1022A>C	XP_005273079.1:p.Gln341Pro
XM_011544026.3:c.1832A>C	XP_011542328.1:p.Gln611Pro
XM_011544028.3:c.1607A>C	XP_011542330.1:p.Gln536Pro
XM_011544030.3:c.998A>C	XP_011542332.1:p.Gln333Pro
XM_017000104.2:c.1814A>C	XP_016855593.1:p.Gln605Pro
XM_017000105.2:c.1706A>C	XP_016855594.1:p.Gln569Pro
XM_024452537.1:c.1745A>C	XP_024308305.1:p.Gln582Pro
XM_024452539.1:c.1745A>C	XP_024308307.1:p.Gln582Pro
XM_024452540.1:c.1745A>C	XP_024308308.1:p.Gln582Pro
XM_024452547.1:c.1649A>C	XP_024308315.1:p.Gln550Pro
XM_024452548.1:c.1745A>C	XP_024308316.1:p.Gln582Pro
XM_024452549.1:c.1412A>C	XP_024308317.1:p.Gln471Pro
XR_002958955.1:n.1985A>C
XR_002958956.1:n.1985A>C
XR_002958965.1:n.1876A>C
NM_006642.5:c.1943A>C MANE Select	NP_006633.1:p.Gln648Pro
NM_001350246.2:c.1040A>C	NP_001337175.1:p.Gln347Pro
NM_001350247.2:c.1040A>C	NP_001337176.1:p.Gln347Pro
NM_001350248.2:c.2039A>C	NP_001337177.1:p.Gln680Pro
NM_001350249.2:c.1649A>C	NP_001337178.1:p.Gln550Pro
NM_001350251.2:c.1040A>C	NP_001337180.1:p.Gln347Pro