Canonical Allele Identifier: CA644622

Gene: IGSF21

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.18365266T>C , CM000663.2:g.18365266T>C	GRCh38
NC_000001.10:g.18691760T>C , CM000663.1:g.18691760T>C	GRCh37
NC_000001.9:g.18564347T>C	NCBI36
NG_027535.1:g.262521T>C
NG_027535.2:g.262521T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032880.5:c.584T>C MANE Select	NP_116269.3:p.Leu195Pro
ENST00000251296.4:c.584T>C MANE Select	ENSP00000251296.1:p.Leu195Pro
NM_032880.4:c.584T>C	NP_116269.3:p.Leu195Pro
ENST00000251296.3:c.584T>C	ENSP00000251296.1:p.Leu195Pro
ENST00000412684.3:n.441T>C
ENST00000497331.2:n.908T>C
XM_011542318.1:c.566T>C	XP_011540620.1:p.Leu189Pro
XM_011542319.1:c.425-11044T>C	XP_011540621.1:n.425-11044T>C
XM_011542319.3:c.425-11044T>C	XP_011540621.1:n.425-11044T>C
XM_017002604.2:c.566T>C	XP_016858093.1:p.Leu189Pro
XM_017002605.1:c.353T>C	XP_016858094.1:p.Leu118Pro
XM_024450444.1:c.425T>C	XP_024306212.1:p.Leu142Pro