Canonical Allele Identifier: CA1607993209
Gene: F13A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6286122G= , CM000668.2:g.6286122G= GRCh38
NC_000006.11:g.6286355G= , CM000668.1:g.6286355G= GRCh37
NC_000006.10:g.6231354G= NCBI36
NG_008107.1:g.39570C= , LRG_549:g.39570C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.319+19229C= MANE Select ENSP00000264870.3:n.319+19229C=
ENST00000264870.7:c.319+19229C= ENSP00000264870.3:n.319+19229C=
ENST00000414279.5:c.319+19229C= ENSP00000413334.1:n.319+19229C=
ENST00000431222.6:c.481+19229C= ENSP00000416295.2:n.481+19229C=
ENST00000479211.1:n.304+19229C=
NM_000129.3:c.319+19229C= , LRG_549t1:c.319+19229C= NP_000120.2:n.319+19229C=
XM_006715010.2:c.319+19229C= XP_006715073.1:n.319+19229C=
XM_011514342.1:c.481+19229C= XP_011512644.1:n.481+19229C=
NM_000129.4:c.319+19229C= MANE Select NP_000120.2:n.319+19229C=
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