Canonical Allele Identifier: CA429731665

Gene: KCNH7

Linked Data

• MyVariant Identifiers: chr2:g.163291799G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162435289G>T , CM000664.2:g.162435289G>T	GRCh38
NC_000002.11:g.163291799G>T , CM000664.1:g.163291799G>T	GRCh37
NC_000002.10:g.163000045G>T	NCBI36
NG_041938.1:g.408459C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.1863C>A MANE Select	ENSP00000331727.5:p.Thr621=
ENST00000328032.8:c.1842C>A	ENSP00000333781.4:p.Thr614=
ENST00000332142.9:c.1863C>A	ENSP00000331727.5:p.Thr621=
ENST00000618399.4:c.1563C>A	ENSP00000482818.1:p.Thr521=
ENST00000621889.1:c.1536C>A	ENSP00000483158.1:p.Thr512=
NM_033272.3:c.1863C>A	NP_150375.2:p.Thr621=
NM_173162.2:c.1842C>A	NP_775185.1:p.Thr614=
XM_011512109.1:c.1887C>A	XP_011510411.1:p.Thr629=
XM_011512109.3:c.1887C>A	XP_011510411.1:p.Thr629=
XM_017005218.2:c.1887C>A	XP_016860707.1:p.Thr629=
XM_017005219.2:c.1863C>A	XP_016860708.1:p.Thr621=
XM_017005220.2:c.1842C>A	XP_016860709.1:p.Thr614=
XM_017005221.2:c.1887C>A	XP_016860710.1:p.Thr629=
NM_033272.4:c.1863C>A MANE Select	NP_150375.2:p.Thr621=
NM_173162.3:c.1842C>A	NP_775185.1:p.Thr614=