Canonical Allele Identifier: CA650476065
Gene: F13A1 HGNC NCBI

Linked Data

COSMIC: COSN22980591
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6286110G>A , CM000668.2:g.6286110G>A GRCh38
NC_000006.11:g.6286343G>A , CM000668.1:g.6286343G>A GRCh37
NC_000006.10:g.6231342G>A NCBI36
NG_008107.1:g.39582C>T , LRG_549:g.39582C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.319+19241C>T MANE Select ENSP00000264870.3:n.319+19241C>T
ENST00000264870.7:c.319+19241C>T ENSP00000264870.3:n.319+19241C>T
ENST00000414279.5:c.319+19241C>T ENSP00000413334.1:n.319+19241C>T
ENST00000431222.6:c.481+19241C>T ENSP00000416295.2:n.481+19241C>T
ENST00000479211.1:n.304+19241C>T
NM_000129.3:c.319+19241C>T , LRG_549t1:c.319+19241C>T NP_000120.2:n.319+19241C>T
XM_006715010.2:c.319+19241C>T XP_006715073.1:n.319+19241C>T
XM_011514342.1:c.481+19241C>T XP_011512644.1:n.481+19241C>T
NM_000129.4:c.319+19241C>T MANE Select NP_000120.2:n.319+19241C>T
Search 100 bp 5'
Search 100 bp 3'