Canonical Allele Identifier: CA362655844
Gene: F13A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145635C>G , CM000668.2:g.6145635C>G GRCh38
NC_000006.11:g.6145868C>G , CM000668.1:g.6145868C>G GRCh37
NC_000006.10:g.6090867C>G NCBI36
NG_008107.1:g.180057G>C , LRG_549:g.180057G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.2183G>C MANE Select ENSP00000264870.3:p.Arg728Thr
ENST00000264870.7:c.2183G>C ENSP00000264870.3:p.Arg728Thr
NM_000129.3:c.2183G>C , LRG_549t1:c.2183G>C NP_000120.2:p.Arg728Thr
XM_006715010.2:c.2183G>C XP_006715073.1:p.Arg728Thr
XM_011514342.1:c.2345G>C XP_011512644.1:p.Arg782Thr
NM_000129.4:c.2183G>C MANE Select NP_000120.2:p.Arg728Thr