Canonical Allele Identifier: CA1607987879
Gene: F13A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6224808T= , CM000668.2:g.6224808T= GRCh38
NC_000006.11:g.6225041T= , CM000668.1:g.6225041T= GRCh37
NC_000006.10:g.6170040T= NCBI36
NG_008107.1:g.100884A= , LRG_549:g.100884A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.851A= MANE Select ENSP00000264870.3:p.Tyr284=
ENST00000264870.7:c.851A= ENSP00000264870.3:p.Tyr284=
ENST00000445223.1:c.1A=
NM_000129.3:c.851A= , LRG_549t1:c.851A= NP_000120.2:p.Tyr284=
XM_006715010.2:c.851A= XP_006715073.1:p.Tyr284=
XM_011514342.1:c.1013A= XP_011512644.1:p.Tyr338=
NM_000129.4:c.851A= MANE Select NP_000120.2:p.Tyr284=