Canonical Allele Identifier: CA362655837
Gene: F13A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145630G>T , CM000668.2:g.6145630G>T GRCh38
NC_000006.11:g.6145863G>T , CM000668.1:g.6145863G>T GRCh37
NC_000006.10:g.6090862G>T NCBI36
NG_008107.1:g.180062C>A , LRG_549:g.180062C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.2188C>A MANE Select ENSP00000264870.3:p.Pro730Thr
ENST00000264870.7:c.2188C>A ENSP00000264870.3:p.Pro730Thr
NM_000129.3:c.2188C>A , LRG_549t1:c.2188C>A NP_000120.2:p.Pro730Thr
XM_006715010.2:c.2188C>A XP_006715073.1:p.Pro730Thr
XM_011514342.1:c.2350C>A XP_011512644.1:p.Pro784Thr
NM_000129.4:c.2188C>A MANE Select NP_000120.2:p.Pro730Thr