Canonical Allele Identifier: CA1607949652
Gene: F13A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145270A= , CM000668.2:g.6145270A= GRCh38
NC_000006.11:g.6145503A= , CM000668.1:g.6145503A= GRCh37
NC_000006.10:g.6090502A= NCBI36
NG_008107.1:g.180422T= , LRG_549:g.180422T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.*349T= MANE Select ENSP00000264870.3:n.*349T=
ENST00000264870.7:c.*349T= ENSP00000264870.3:n.*349T=
NM_000129.3:c.*349T= , LRG_549t1:c.*349T= NP_000120.2:n.*349T=
XM_006715010.2:c.*349T= XP_006715073.1:n.*349T=
XM_011514342.1:c.*349T= XP_011512644.1:n.*349T=
NM_000129.4:c.*349T= MANE Select NP_000120.2:n.*349T=