Canonical Allele Identifier: CA345667915

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589852G>T (hg19) ; chr1:g.243426550G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426550G>T , CM000663.2:g.243426550G>T	GRCh38
NC_000001.10:g.243589852G>T , CM000663.1:g.243589852G>T	GRCh37
NC_000001.9:g.241656475G>T	NCBI36
NG_027811.1:g.175546G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1977G>T MANE Select	ENSP00000355499.3:p.Met659Ile
ENST00000366541.7:c.1977G>T	ENSP00000355499.3:p.Met659Ile
ENST00000435549.1:c.1080G>T	ENSP00000410200.1:p.Met360Ile
ENST00000463042.1:n.184G>T
NM_006642.3:c.1977G>T	NP_006633.1:p.Met659Ile
XM_005273013.3:c.1848G>T	XP_005273070.1:p.Met616Ile
XM_005273018.1:c.1554G>T	XP_005273075.1:p.Met518Ile
XM_005273021.3:c.1074G>T	XP_005273078.1:p.Met358Ile
XM_005273022.2:c.1056G>T	XP_005273079.1:p.Met352Ile
XM_006711727.2:c.2007G>T	XP_006711790.1:p.Met669Ile
XM_006711728.2:c.1878G>T	XP_006711791.1:p.Met626Ile
XM_006711729.2:c.1818G>T	XP_006711792.1:p.Met606Ile
XM_011544021.1:c.2103G>T	XP_011542323.1:p.Met701Ile
XM_011544022.1:c.2073G>T	XP_011542324.1:p.Met691Ile
XM_011544023.1:c.2103G>T	XP_011542325.1:p.Met701Ile
XM_011544024.1:c.2103G>T	XP_011542326.1:p.Met701Ile
XM_011544025.1:c.1914G>T	XP_011542327.1:p.Met638Ile
XM_011544026.1:c.1866G>T	XP_011542328.1:p.Met622Ile
XM_011544027.1:c.1689G>T	XP_011542329.1:p.Met563Ile
XM_011544028.1:c.1641G>T	XP_011542330.1:p.Met547Ile
XM_011544030.1:c.1032G>T	XP_011542332.1:p.Met344Ile
XR_949128.1:n.2127G>T
NM_001350246.1:c.1074G>T	NP_001337175.1:p.Met358Ile
NM_001350247.1:c.1074G>T	NP_001337176.1:p.Met358Ile
NM_001350248.1:c.2073G>T	NP_001337177.1:p.Met691Ile
NM_001350249.1:c.1683G>T	NP_001337178.1:p.Met561Ile
NM_001350251.1:c.1074G>T	NP_001337180.1:p.Met358Ile
NM_006642.4:c.1977G>T	NP_006633.1:p.Met659Ile
XM_005273013.5:c.1848G>T	XP_005273070.1:p.Met616Ile
XM_005273018.2:c.1554G>T	XP_005273075.1:p.Met518Ile
XM_005273022.4:c.1056G>T	XP_005273079.1:p.Met352Ile
XM_011544026.3:c.1866G>T	XP_011542328.1:p.Met622Ile
XM_011544028.3:c.1641G>T	XP_011542330.1:p.Met547Ile
XM_011544030.3:c.1032G>T	XP_011542332.1:p.Met344Ile
XM_017000104.2:c.1848G>T	XP_016855593.1:p.Met616Ile
XM_017000105.2:c.1740G>T	XP_016855594.1:p.Met580Ile
XM_024452537.1:c.1779G>T	XP_024308305.1:p.Met593Ile
XM_024452539.1:c.1779G>T	XP_024308307.1:p.Met593Ile
XM_024452540.1:c.1779G>T	XP_024308308.1:p.Met593Ile
XM_024452547.1:c.1683G>T	XP_024308315.1:p.Met561Ile
XM_024452548.1:c.1779G>T	XP_024308316.1:p.Met593Ile
XM_024452549.1:c.1446G>T	XP_024308317.1:p.Met482Ile
XR_002958955.1:n.2019G>T
XR_002958956.1:n.2019G>T
XR_002958965.1:n.1910G>T
NM_006642.5:c.1977G>T MANE Select	NP_006633.1:p.Met659Ile
NM_001350246.2:c.1074G>T	NP_001337175.1:p.Met358Ile
NM_001350247.2:c.1074G>T	NP_001337176.1:p.Met358Ile
NM_001350248.2:c.2073G>T	NP_001337177.1:p.Met691Ile
NM_001350249.2:c.1683G>T	NP_001337178.1:p.Met561Ile
NM_001350251.2:c.1074G>T	NP_001337180.1:p.Met358Ile