Canonical Allele Identifier: CA1607949572
Gene: F13A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145056G= , CM000668.2:g.6145056G= GRCh38
NC_000006.11:g.6145289G= , CM000668.1:g.6145289G= GRCh37
NC_000006.10:g.6090288G= NCBI36
NG_008107.1:g.180636C= , LRG_549:g.180636C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.*563C= MANE Select ENSP00000264870.3:n.*563C=
ENST00000264870.7:c.*563C= ENSP00000264870.3:n.*563C=
NM_000129.3:c.*563C= , LRG_549t1:c.*563C= NP_000120.2:n.*563C=
XM_006715010.2:c.*563C= XP_006715073.1:n.*563C=
XM_011514342.1:c.*563C= XP_011512644.1:n.*563C=
NM_000129.4:c.*563C= MANE Select NP_000120.2:n.*563C=
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