Canonical Allele Identifier: CA345667868

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589829C>G (hg19) ; chr1:g.243426527C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426527C>G , CM000663.2:g.243426527C>G	GRCh38
NC_000001.10:g.243589829C>G , CM000663.1:g.243589829C>G	GRCh37
NC_000001.9:g.241656452C>G	NCBI36
NG_027811.1:g.175523C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1954C>G MANE Select	ENSP00000355499.3:p.His652Asp
ENST00000366541.7:c.1954C>G	ENSP00000355499.3:p.His652Asp
ENST00000435549.1:c.1057C>G	ENSP00000410200.1:p.His353Asp
ENST00000463042.1:n.161C>G
NM_006642.3:c.1954C>G	NP_006633.1:p.His652Asp
XM_005273013.3:c.1825C>G	XP_005273070.1:p.His609Asp
XM_005273018.1:c.1531C>G	XP_005273075.1:p.His511Asp
XM_005273021.3:c.1051C>G	XP_005273078.1:p.His351Asp
XM_005273022.2:c.1033C>G	XP_005273079.1:p.His345Asp
XM_006711727.2:c.1984C>G	XP_006711790.1:p.His662Asp
XM_006711728.2:c.1855C>G	XP_006711791.1:p.His619Asp
XM_006711729.2:c.1795C>G	XP_006711792.1:p.His599Asp
XM_011544021.1:c.2080C>G	XP_011542323.1:p.His694Asp
XM_011544022.1:c.2050C>G	XP_011542324.1:p.His684Asp
XM_011544023.1:c.2080C>G	XP_011542325.1:p.His694Asp
XM_011544024.1:c.2080C>G	XP_011542326.1:p.His694Asp
XM_011544025.1:c.1891C>G	XP_011542327.1:p.His631Asp
XM_011544026.1:c.1843C>G	XP_011542328.1:p.His615Asp
XM_011544027.1:c.1666C>G	XP_011542329.1:p.His556Asp
XM_011544028.1:c.1618C>G	XP_011542330.1:p.His540Asp
XM_011544030.1:c.1009C>G	XP_011542332.1:p.His337Asp
XR_949128.1:n.2104C>G
NM_001350246.1:c.1051C>G	NP_001337175.1:p.His351Asp
NM_001350247.1:c.1051C>G	NP_001337176.1:p.His351Asp
NM_001350248.1:c.2050C>G	NP_001337177.1:p.His684Asp
NM_001350249.1:c.1660C>G	NP_001337178.1:p.His554Asp
NM_001350251.1:c.1051C>G	NP_001337180.1:p.His351Asp
NM_006642.4:c.1954C>G	NP_006633.1:p.His652Asp
XM_005273013.5:c.1825C>G	XP_005273070.1:p.His609Asp
XM_005273018.2:c.1531C>G	XP_005273075.1:p.His511Asp
XM_005273022.4:c.1033C>G	XP_005273079.1:p.His345Asp
XM_011544026.3:c.1843C>G	XP_011542328.1:p.His615Asp
XM_011544028.3:c.1618C>G	XP_011542330.1:p.His540Asp
XM_011544030.3:c.1009C>G	XP_011542332.1:p.His337Asp
XM_017000104.2:c.1825C>G	XP_016855593.1:p.His609Asp
XM_017000105.2:c.1717C>G	XP_016855594.1:p.His573Asp
XM_024452537.1:c.1756C>G	XP_024308305.1:p.His586Asp
XM_024452539.1:c.1756C>G	XP_024308307.1:p.His586Asp
XM_024452540.1:c.1756C>G	XP_024308308.1:p.His586Asp
XM_024452547.1:c.1660C>G	XP_024308315.1:p.His554Asp
XM_024452548.1:c.1756C>G	XP_024308316.1:p.His586Asp
XM_024452549.1:c.1423C>G	XP_024308317.1:p.His475Asp
XR_002958955.1:n.1996C>G
XR_002958956.1:n.1996C>G
XR_002958965.1:n.1887C>G
NM_006642.5:c.1954C>G MANE Select	NP_006633.1:p.His652Asp
NM_001350246.2:c.1051C>G	NP_001337175.1:p.His351Asp
NM_001350247.2:c.1051C>G	NP_001337176.1:p.His351Asp
NM_001350248.2:c.2050C>G	NP_001337177.1:p.His684Asp
NM_001350249.2:c.1660C>G	NP_001337178.1:p.His554Asp
NM_001350251.2:c.1051C>G	NP_001337180.1:p.His351Asp