Canonical Allele Identifier: CA633277338

Gene: KCNN4

Linked Data

• dbSNP Id: rs1273555735
• gnomAD v2: 19-44280657-G-A
• gnomAD v3: 19-43776505-G-A
• gnomAD v4: 19-43776505-G-A
• MyVariant Identifiers: chr19:g.44280657G>A (hg19) ; chr19:g.43776505G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776505G>A , CM000681.2:g.43776505G>A	GRCh38
NC_000019.9:g.44280657G>A , CM000681.1:g.44280657G>A	GRCh37
NC_000019.8:g.48972497G>A	NCBI36
NG_052672.1:g.10635C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+36C>T MANE Select	ENSP00000496939.1:n.255+36C>T
ENST00000262888.7:c.255+36C>T	ENSP00000262888.3:n.255+36C>T
ENST00000599107.1:n.286+36C>T
ENST00000599720.5:c.159+4198C>T	ENSP00000472513.1:n.159+4198C>T
ENST00000615047.4:c.70+36C>T	ENSP00000485014.1:n.70+36C>T
NM_002250.2:c.255+36C>T	NP_002241.1:n.255+36C>T
XM_005258882.2:c.160-1886C>T	XP_005258939.1:n.160-1886C>T
XM_005258883.2:c.70+36C>T	XP_005258940.1:n.70+36C>T
XM_011526938.1:c.255+36C>T	XP_011525240.1:n.255+36C>T
XR_935823.1:n.1533+36C>T
XR_002958313.1:n.1533+36C>T
NM_002250.3:c.255+36C>T MANE Select	NP_002241.1:n.255+36C>T