Canonical Allele Identifier: CA1607949586
Gene: F13A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145084A= , CM000668.2:g.6145084A= GRCh38
NC_000006.11:g.6145317A= , CM000668.1:g.6145317A= GRCh37
NC_000006.10:g.6090316A= NCBI36
NG_008107.1:g.180608T= , LRG_549:g.180608T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.*535T= MANE Select ENSP00000264870.3:n.*535T=
ENST00000264870.7:c.*535T= ENSP00000264870.3:n.*535T=
NM_000129.3:c.*535T= , LRG_549t1:c.*535T= NP_000120.2:n.*535T=
XM_006715010.2:c.*535T= XP_006715073.1:n.*535T=
XM_011514342.1:c.*535T= XP_011512644.1:n.*535T=
NM_000129.4:c.*535T= MANE Select NP_000120.2:n.*535T=