Canonical Allele Identifier: CA1608030281
Gene: F13A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6318488G= , CM000668.2:g.6318488G= GRCh38
NC_000006.11:g.6318721G= , CM000668.1:g.6318721G= GRCh37
NC_000006.10:g.6263720G= NCBI36
NG_008107.1:g.7204C= , LRG_549:g.7204C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.130+47C= MANE Select ENSP00000264870.3:n.130+47C=
ENST00000264870.7:c.130+47C= ENSP00000264870.3:n.130+47C=
ENST00000414279.5:c.130+47C= ENSP00000413334.1:n.130+47C=
ENST00000431222.6:c.292+47C= ENSP00000416295.2:n.292+47C=
ENST00000451619.1:c.204+47C=
NM_000129.3:c.130+47C= , LRG_549t1:c.130+47C= NP_000120.2:n.130+47C=
XM_006715010.2:c.130+47C= XP_006715073.1:n.130+47C=
XM_011514342.1:c.292+47C= XP_011512644.1:n.292+47C=
NM_000129.4:c.130+47C= MANE Select NP_000120.2:n.130+47C=
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