Canonical Allele Identifier: CA1191535

Gene: TAGLN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159920487T>C , CM000663.2:g.159920487T>C	GRCh38
NC_000001.10:g.159890277T>C , CM000663.1:g.159890277T>C	GRCh37
NC_000001.9:g.158156901T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368097.9:c.23A>G MANE Select	ENSP00000357077.5:p.Tyr8Cys
ENST00000320307.8:c.23A>G	ENSP00000357075.1:p.Tyr8Cys
ENST00000368096.5:c.86A>G	ENSP00000357076.1:p.Tyr29Cys
ENST00000368097.8:c.23A>G	ENSP00000357077.4:p.Tyr8Cys
ENST00000397334.2:c.23A>G	ENSP00000412429.1:p.Tyr8Cys
ENST00000478033.1:n.93A>G
NM_001277223.1:c.23A>G	NP_001264152.1:p.Tyr8Cys
NM_001277224.1:c.86A>G	NP_001264153.1:p.Tyr29Cys
NM_003564.2:c.23A>G	NP_003555.1:p.Tyr8Cys
NM_001277223.2:c.23A>G	NP_001264152.1:p.Tyr8Cys
NM_001277224.2:c.86A>G	NP_001264153.1:p.Tyr29Cys
NM_003564.3:c.23A>G MANE Select	NP_003555.1:p.Tyr8Cys