Canonical Allele Identifier: CA155900631
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs140074877
gnomAD v2: 7-27135112-G-C
gnomAD v3: 7-27095493-G-C
gnomAD v4: 7-27095493-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095493G>C , CM000669.2:g.27095493G>C GRCh38
NC_000007.13:g.27135112G>C , CM000669.1:g.27135112G>C GRCh37
NC_000007.12:g.27101637G>C NCBI36
NG_011813.1:g.5514C>G
NG_033087.1:g.4400G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.420C>G MANE Select ENSP00000494260.2:p.Val140=
ENST00000343060.4:c.420C>G ENSP00000343246.4:p.Val140=
ENST00000355633.5:c.354+66C>G ENSP00000347851.5:n.354+66C>G
NM_005522.4:c.420C>G NP_005513.1:p.Val140=
NM_153620.2:c.354+66C>G NP_705873.2:n.354+66C>G
NM_005522.5:c.420C>G MANE Select NP_005513.2:p.Val140=
NM_153620.3:c.354+66C>G NP_705873.3:n.354+66C>G