Canonical Allele Identifier: CA1607973446
Gene: F13A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6182179T= , CM000668.2:g.6182179T= GRCh38
NC_000006.11:g.6182412T= , CM000668.1:g.6182412T= GRCh37
NC_000006.10:g.6127411T= NCBI36
NG_008107.1:g.143513A= , LRG_549:g.143513A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.1306-38A= MANE Select ENSP00000264870.3:n.1306-38A=
ENST00000264870.7:c.1306-38A= ENSP00000264870.3:n.1306-38A=
NM_000129.3:c.1306-38A= , LRG_549t1:c.1306-38A= NP_000120.2:n.1306-38A=
XM_006715010.2:c.1306-38A= XP_006715073.1:n.1306-38A=
XM_011514342.1:c.1468-38A= XP_011512644.1:n.1468-38A=
NM_000129.4:c.1306-38A= MANE Select NP_000120.2:n.1306-38A=
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