Canonical Allele Identifier: CA349220810

Gene: KCNH7

Linked Data

• MyVariant Identifiers: chr2:g.163291786T>A (hg19) ; chr2:g.162435276T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162435276T>A , CM000664.2:g.162435276T>A	GRCh38
NC_000002.11:g.163291786T>A , CM000664.1:g.163291786T>A	GRCh37
NC_000002.10:g.163000032T>A	NCBI36
NG_041938.1:g.408472A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.1876A>T MANE Select	ENSP00000331727.5:p.Thr626Ser
ENST00000328032.8:c.1855A>T	ENSP00000333781.4:p.Thr619Ser
ENST00000332142.9:c.1876A>T	ENSP00000331727.5:p.Thr626Ser
ENST00000618399.4:c.1576A>T	ENSP00000482818.1:p.Thr526Ser
ENST00000621889.1:c.1549A>T	ENSP00000483158.1:p.Thr517Ser
NM_033272.3:c.1876A>T	NP_150375.2:p.Thr626Ser
NM_173162.2:c.1855A>T	NP_775185.1:p.Thr619Ser
XM_011512109.1:c.1900A>T	XP_011510411.1:p.Thr634Ser
XM_011512109.3:c.1900A>T	XP_011510411.1:p.Thr634Ser
XM_017005218.2:c.1900A>T	XP_016860707.1:p.Thr634Ser
XM_017005219.2:c.1876A>T	XP_016860708.1:p.Thr626Ser
XM_017005220.2:c.1855A>T	XP_016860709.1:p.Thr619Ser
XM_017005221.2:c.1900A>T	XP_016860710.1:p.Thr634Ser
NM_033272.4:c.1876A>T MANE Select	NP_150375.2:p.Thr626Ser
NM_173162.3:c.1855A>T	NP_775185.1:p.Thr619Ser