Canonical Allele Identifier: CA1607949739
Gene: F13A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145479G= , CM000668.2:g.6145479G= GRCh38
NC_000006.11:g.6145712G= , CM000668.1:g.6145712G= GRCh37
NC_000006.10:g.6090711G= NCBI36
NG_008107.1:g.180213C= , LRG_549:g.180213C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.*140C= MANE Select ENSP00000264870.3:n.*140C=
ENST00000264870.7:c.*140C= ENSP00000264870.3:n.*140C=
NM_000129.3:c.*140C= , LRG_549t1:c.*140C= NP_000120.2:n.*140C=
XM_006715010.2:c.*140C= XP_006715073.1:n.*140C=
XM_011514342.1:c.*140C= XP_011512644.1:n.*140C=
NM_000129.4:c.*140C= MANE Select NP_000120.2:n.*140C=