Canonical Allele Identifier: CA349221131

Gene: KCNH7

Linked Data

• MyVariant Identifiers: chr2:g.163291927G>T (hg19) ; chr2:g.162435417G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162435417G>T , CM000664.2:g.162435417G>T	GRCh38
NC_000002.11:g.163291927G>T , CM000664.1:g.163291927G>T	GRCh37
NC_000002.10:g.163000173G>T	NCBI36
NG_041938.1:g.408331C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.1735C>A MANE Select	ENSP00000331727.5:p.Pro579Thr
ENST00000328032.8:c.1714C>A	ENSP00000333781.4:p.Pro572Thr
ENST00000332142.9:c.1735C>A	ENSP00000331727.5:p.Pro579Thr
ENST00000618399.4:c.1435C>A	ENSP00000482818.1:p.Pro479Thr
ENST00000621889.1:c.1408C>A	ENSP00000483158.1:p.Pro470Thr
NM_033272.3:c.1735C>A	NP_150375.2:p.Pro579Thr
NM_173162.2:c.1714C>A	NP_775185.1:p.Pro572Thr
XM_011512109.1:c.1759C>A	XP_011510411.1:p.Pro587Thr
XM_011512109.3:c.1759C>A	XP_011510411.1:p.Pro587Thr
XM_017005218.2:c.1759C>A	XP_016860707.1:p.Pro587Thr
XM_017005219.2:c.1735C>A	XP_016860708.1:p.Pro579Thr
XM_017005220.2:c.1714C>A	XP_016860709.1:p.Pro572Thr
XM_017005221.2:c.1759C>A	XP_016860710.1:p.Pro587Thr
NM_033272.4:c.1735C>A MANE Select	NP_150375.2:p.Pro579Thr
NM_173162.3:c.1714C>A	NP_775185.1:p.Pro572Thr