Canonical Allele Identifier: CA1607949746
Gene: F13A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145493A= , CM000668.2:g.6145493A= GRCh38
NC_000006.11:g.6145726A= , CM000668.1:g.6145726A= GRCh37
NC_000006.10:g.6090725A= NCBI36
NG_008107.1:g.180199T= , LRG_549:g.180199T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.*126T= MANE Select ENSP00000264870.3:n.*126T=
ENST00000264870.7:c.*126T= ENSP00000264870.3:n.*126T=
NM_000129.3:c.*126T= , LRG_549t1:c.*126T= NP_000120.2:n.*126T=
XM_006715010.2:c.*126T= XP_006715073.1:n.*126T=
XM_011514342.1:c.*126T= XP_011512644.1:n.*126T=
NM_000129.4:c.*126T= MANE Select NP_000120.2:n.*126T=