Canonical Allele Identifier: CA619410572

Gene: HCN4

Linked Data

• dbSNP Id: rs1224069282
• gnomAD v2: 15-73614802-G-GAAAGAGAAAAGAGAAAAGAAAAGA
• gnomAD v3: 15-73322461-G-GAAAGAGAAAAGAGAAAAGAAAAGA
• gnomAD v4: 15-73322461-G-GAAAGAGAAAAGAGAAAAGAAAAGA
• MyVariant Identifiers: chr15:g.73614802_73614803insAAAGAGAAAAGAGAAAAGAAAAGA (hg19) ; chr15:g.73322461_73322462insAAAGAGAAAAGAGAAAAGAAAAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322462_73322463insAAGAGAAAAGAGAAAAGAAAAGAA , CM000677.2:g.73322462_73322463insAAGAGAAAAGAGAAAAGAAAAGAA	GRCh38
NC_000015.9:g.73614803_73614804insAAGAGAAAAGAGAAAAGAAAAGAA , CM000677.1:g.73614803_73614804insAAGAGAAAAGAGAAAAGAAAAGAA	GRCh37
NC_000015.8:g.71401856_71401857insAAGAGAAAAGAGAAAAGAAAAGAA	NCBI36
NG_009063.1:g.51803_51804insTCTTTTCTTTTCTCTTTTCTCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT MANE Select	ENSP00000261917.3:n.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT
ENST00000261917.3:c.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT	ENSP00000261917.3:n.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT
NM_005477.2:c.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT	NP_005468.1:n.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT
XM_011521148.1:c.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT	XP_011519450.1:n.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT
XM_011521148.2:c.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT	XP_011519450.1:n.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT
NM_005477.3:c.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT MANE Select	NP_005468.1:n.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT