Canonical Allele Identifier: CA1607949711
Gene: F13A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145400T= , CM000668.2:g.6145400T= GRCh38
NC_000006.11:g.6145633T= , CM000668.1:g.6145633T= GRCh37
NC_000006.10:g.6090632T= NCBI36
NG_008107.1:g.180292A= , LRG_549:g.180292A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.*219A= MANE Select ENSP00000264870.3:n.*219A=
ENST00000264870.7:c.*219A= ENSP00000264870.3:n.*219A=
NM_000129.3:c.*219A= , LRG_549t1:c.*219A= NP_000120.2:n.*219A=
XM_006715010.2:c.*219A= XP_006715073.1:n.*219A=
XM_011514342.1:c.*219A= XP_011512644.1:n.*219A=
NM_000129.4:c.*219A= MANE Select NP_000120.2:n.*219A=
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