Canonical Allele Identifier: CA367068665
Gene: HOXA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095519A>G , CM000669.2:g.27095519A>G GRCh38
NC_000007.13:g.27135138A>G , CM000669.1:g.27135138A>G GRCh37
NC_000007.12:g.27101663A>G NCBI36
NG_011813.1:g.5488T>C
NG_033087.1:g.4426A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.394T>C MANE Select ENSP00000494260.2:p.Ser132Pro
ENST00000343060.4:c.394T>C ENSP00000343246.4:p.Ser132Pro
ENST00000355633.5:c.354+40T>C ENSP00000347851.5:n.354+40T>C
NM_005522.4:c.394T>C NP_005513.1:p.Ser132Pro
NM_153620.2:c.354+40T>C NP_705873.2:n.354+40T>C
NM_005522.5:c.394T>C MANE Select NP_005513.2:p.Ser132Pro
NM_153620.3:c.354+40T>C NP_705873.3:n.354+40T>C