Canonical Allele Identifier: CA2337652611

Gene: KCNN4

Linked Data

• dbSNP Id: rs1349256489
• gnomAD v4: 19-43769716-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769716C>T , CM000681.2:g.43769716C>T	GRCh38
NC_000019.9:g.44273868C>T , CM000681.1:g.44273868C>T	GRCh37
NC_000019.8:g.48965708C>T	NCBI36
NG_052672.1:g.17424G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.552+3G>A
ENST00000648053.1:n.362+3G>A
ENST00000648319.1:c.930+3G>A MANE Select	ENSP00000496939.1:n.930+3G>A
ENST00000262888.7:c.930+3G>A	ENSP00000262888.3:n.930+3G>A
ENST00000598836.1:c.109+3G>A
ENST00000599720.5:c.*200+3G>A	ENSP00000472513.1:n.*200+3G>A
ENST00000600408.1:c.219+3G>A	ENSP00000472510.1:n.219+3G>A
ENST00000601549.1:n.239+3G>A
ENST00000615047.4:c.534+3G>A	ENSP00000485014.1:n.534+3G>A
NM_002250.2:c.930+3G>A	NP_002241.1:n.930+3G>A
XM_005258882.2:c.834+3G>A	XP_005258939.1:n.834+3G>A
XM_005258883.2:c.741+3G>A	XP_005258940.1:n.741+3G>A
XR_935823.1:n.2176+3G>A
XR_002958313.1:n.2322+3G>A
NM_002250.3:c.930+3G>A MANE Select	NP_002241.1:n.930+3G>A