Canonical Allele Identifier: CA4195988

Gene: HOXA1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095694_27095695insTGATGG , CM000669.2:g.27095694_27095695insTGATGG	GRCh38
NC_000007.13:g.27135313_27135314insTGATGG , CM000669.1:g.27135313_27135314insTGATGG	GRCh37
NC_000007.12:g.27101838_27101839insTGATGG	NCBI36
NG_011813.1:g.5315_5316insTCACCA
NG_033087.1:g.4601_4602insTGATGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643460.2:c.221_222insTCACCA MANE Select	ENSP00000494260.2:p.His74_Pro75insHisHis
ENST00000343060.4:c.221_222insTCACCA	ENSP00000343246.4:p.His74_Pro75insHisHis
ENST00000355633.5:c.221_222insTCACCA	ENSP00000347851.5:p.His74_Pro75insHisHis
NM_005522.4:c.221_222insTCACCA	NP_005513.1:p.His74_Pro75insHisHis
NM_153620.2:c.221_222insTCACCA	NP_705873.2:p.His74_Pro75insHisHis
NM_005522.5:c.221_222insTCACCA MANE Select	NP_005513.2:p.His74_Pro75insHisHis
NM_153620.3:c.221_222insTCACCA	NP_705873.3:p.His74_Pro75insHisHis