Canonical Allele Identifier: CA1607949659
Gene: F13A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145294A= , CM000668.2:g.6145294A= GRCh38
NC_000006.11:g.6145527A= , CM000668.1:g.6145527A= GRCh37
NC_000006.10:g.6090526A= NCBI36
NG_008107.1:g.180398T= , LRG_549:g.180398T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.*325T= MANE Select ENSP00000264870.3:n.*325T=
ENST00000264870.7:c.*325T= ENSP00000264870.3:n.*325T=
NM_000129.3:c.*325T= , LRG_549t1:c.*325T= NP_000120.2:n.*325T=
XM_006715010.2:c.*325T= XP_006715073.1:n.*325T=
XM_011514342.1:c.*325T= XP_011512644.1:n.*325T=
NM_000129.4:c.*325T= MANE Select NP_000120.2:n.*325T=
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