Canonical Allele Identifier: CA362739900
Gene: F13A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6224709A>C , CM000668.2:g.6224709A>C GRCh38
NC_000006.11:g.6224942A>C , CM000668.1:g.6224942A>C GRCh37
NC_000006.10:g.6169941A>C NCBI36
NG_008107.1:g.100983T>G , LRG_549:g.100983T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.950T>G MANE Select ENSP00000264870.3:p.Val317Gly
ENST00000264870.7:c.950T>G ENSP00000264870.3:p.Val317Gly
ENST00000445223.1:c.100T>G
NM_000129.3:c.950T>G , LRG_549t1:c.950T>G NP_000120.2:p.Val317Gly
XM_006715010.2:c.950T>G XP_006715073.1:p.Val317Gly
XM_011514342.1:c.1112T>G XP_011512644.1:p.Val371Gly
NM_000129.4:c.950T>G MANE Select NP_000120.2:p.Val317Gly