Canonical Allele Identifier: CA1607993210
Gene: F13A1 HGNC NCBI

Linked Data

dbSNP Id: rs1758136518
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Genomic Alleles

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

Transcript Alleles

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