Canonical Allele Identifier: CA1607949676
Gene: F13A1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145334T= , CM000668.2:g.6145334T= GRCh38
NC_000006.11:g.6145567T= , CM000668.1:g.6145567T= GRCh37
NC_000006.10:g.6090566T= NCBI36
NG_008107.1:g.180358A= , LRG_549:g.180358A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.*285A= MANE Select ENSP00000264870.3:n.*285A=
ENST00000264870.7:c.*285A= ENSP00000264870.3:n.*285A=
NM_000129.3:c.*285A= , LRG_549t1:c.*285A= NP_000120.2:n.*285A=
XM_006715010.2:c.*285A= XP_006715073.1:n.*285A=
XM_011514342.1:c.*285A= XP_011512644.1:n.*285A=
NM_000129.4:c.*285A= MANE Select NP_000120.2:n.*285A=
Search 100 bp 5'
Search 100 bp 3'