Canonical Allele Identifier: CA811095254

Gene: HCN1

Linked Data

• dbSNP Id: rs1156935751
• MyVariant Identifiers: chr5:g.45461877_45461884del (hg19) ; chr5:g.45461775_45461782del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45461776_45461783del , CM000667.2:g.45461776_45461783del	GRCh38
NC_000005.9:g.45461878_45461885del , CM000667.1:g.45461878_45461885del	GRCh37
NC_000005.8:g.45497635_45497642del	NCBI36
NG_042183.1:g.239337_239344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.1011+64_1011+71del MANE Select	ENSP00000307342.4:n.1011+64_1011+71del
ENST00000637305.1:n.174+64_174+71del
ENST00000673735.1:c.1011+64_1011+71del	ENSP00000501107.1:n.1011+64_1011+71del
ENST00000303230.5:c.1011+64_1011+71del	ENSP00000307342.4:n.1011+64_1011+71del
NM_021072.3:c.1011+64_1011+71del	NP_066550.2:n.1011+64_1011+71del
NM_021072.4:c.1011+64_1011+71del MANE Select	NP_066550.2:n.1011+64_1011+71del