Canonical Allele Identifier: CA448645832

Gene: F13A1

Linked Data

• MyVariant Identifiers: chr6:g.6224991A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6224758A>G , CM000668.2:g.6224758A>G	GRCh38
NC_000006.11:g.6224991A>G , CM000668.1:g.6224991A>G	GRCh37
NC_000006.10:g.6169990A>G	NCBI36
NG_008107.1:g.100934T>C , LRG_549:g.100934T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.901T>C MANE Select	ENSP00000264870.3:p.Leu301=
ENST00000264870.7:c.901T>C	ENSP00000264870.3:p.Leu301=
ENST00000445223.1:c.51T>C
NM_000129.3:c.901T>C , LRG_549t1:c.901T>C	NP_000120.2:p.Leu301=
XM_006715010.2:c.901T>C	XP_006715073.1:p.Leu301=
XM_011514342.1:c.1063T>C	XP_011512644.1:p.Leu355=
NM_000129.4:c.901T>C MANE Select	NP_000120.2:p.Leu301=