Canonical Allele Identifier: CA1607987897
Gene: F13A1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6224871C= , CM000668.2:g.6224871C= GRCh38
NC_000006.11:g.6225104C= , CM000668.1:g.6225104C= GRCh37
NC_000006.10:g.6170103C= NCBI36
NG_008107.1:g.100821G= , LRG_549:g.100821G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.799-11G= MANE Select ENSP00000264870.3:n.799-11G=
ENST00000264870.7:c.799-11G= ENSP00000264870.3:n.799-11G=
NM_000129.3:c.799-11G= , LRG_549t1:c.799-11G= NP_000120.2:n.799-11G=
XM_006715010.2:c.799-11G= XP_006715073.1:n.799-11G=
XM_011514342.1:c.961-11G= XP_011512644.1:n.961-11G=
NM_000129.4:c.799-11G= MANE Select NP_000120.2:n.799-11G=
Search 100 bp 5'
Search 100 bp 3'