Canonical Allele Identifier: CA1607973381
Gene: F13A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6182004A= , CM000668.2:g.6182004A= GRCh38
NC_000006.11:g.6182237A= , CM000668.1:g.6182237A= GRCh37
NC_000006.10:g.6127236A= NCBI36
NG_008107.1:g.143688T= , LRG_549:g.143688T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.1443T= MANE Select ENSP00000264870.3:p.Thr481=
ENST00000264870.7:c.1443T= ENSP00000264870.3:p.Thr481=
NM_000129.3:c.1443T= , LRG_549t1:c.1443T= NP_000120.2:p.Thr481=
XM_006715010.2:c.1443T= XP_006715073.1:p.Thr481=
XM_011514342.1:c.1605T= XP_011512644.1:p.Thr535=
NM_000129.4:c.1443T= MANE Select NP_000120.2:p.Thr481=