Canonical Allele Identifier: CA1085617056
Gene: F13A1 HGNC NCBI

Linked Data

dbSNP Id: rs1757580922
gnomAD v3: 6-6248278-T-TAAC
gnomAD v4: 6-6248278-T-TAAC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6248280_6248282dup , CM000668.2:g.6248280_6248282dup GRCh38
NC_000006.11:g.6248513_6248515dup , CM000668.1:g.6248513_6248515dup GRCh37
NC_000006.10:g.6193512_6193514dup NCBI36
NG_008107.1:g.77411_77413dup , LRG_549:g.77411_77413dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.798+31_798+33dup MANE Select ENSP00000264870.3:n.798+31_798+33dup
ENST00000264870.7:c.798+31_798+33dup ENSP00000264870.3:n.798+31_798+33dup
NM_000129.3:c.798+31_798+33dup , LRG_549t1:c.798+31_798+33dup NP_000120.2:n.798+31_798+33dup
XM_006715010.2:c.798+31_798+33dup XP_006715073.1:n.798+31_798+33dup
XM_011514342.1:c.960+31_960+33dup XP_011512644.1:n.960+31_960+33dup
NM_000129.4:c.798+31_798+33dup MANE Select NP_000120.2:n.798+31_798+33dup
Search 100 bp 5'
Search 100 bp 3'