Canonical Allele Identifier: CA448640489

Gene: F13A1

Linked Data

• MyVariant Identifiers: chr6:g.6182264T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6182031T>C , CM000668.2:g.6182031T>C	GRCh38
NC_000006.11:g.6182264T>C , CM000668.1:g.6182264T>C	GRCh37
NC_000006.10:g.6127263T>C	NCBI36
NG_008107.1:g.143661A>G , LRG_549:g.143661A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264870.8:c.1416A>G MANE Select	ENSP00000264870.3:p.Gly472=
ENST00000264870.7:c.1416A>G	ENSP00000264870.3:p.Gly472=
NM_000129.3:c.1416A>G , LRG_549t1:c.1416A>G	NP_000120.2:p.Gly472=
XM_006715010.2:c.1416A>G	XP_006715073.1:p.Gly472=
XM_011514342.1:c.1578A>G	XP_011512644.1:p.Gly526=
NM_000129.4:c.1416A>G MANE Select	NP_000120.2:p.Gly472=