Canonical Allele Identifier: CA448498812

Gene: F13A1

Linked Data

• MyVariant Identifiers: chr6:g.6167739C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6167506C>A , CM000668.2:g.6167506C>A	GRCh38
NC_000006.11:g.6167739C>A , CM000668.1:g.6167739C>A	GRCh37
NC_000006.10:g.6112738C>A	NCBI36
NG_008107.1:g.158186G>T , LRG_549:g.158186G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264870.8:c.1860G>T MANE Select	ENSP00000264870.3:p.Leu620=
ENST00000264870.7:c.1860G>T	ENSP00000264870.3:p.Leu620=
NM_000129.3:c.1860G>T , LRG_549t1:c.1860G>T	NP_000120.2:p.Leu620=
XM_006715010.2:c.1860G>T	XP_006715073.1:p.Leu620=
XM_011514342.1:c.2022G>T	XP_011512644.1:p.Leu674=
NM_000129.4:c.1860G>T MANE Select	NP_000120.2:p.Leu620=