Canonical Allele Identifier: CA633277309

Gene: KCNN4

Linked Data

• dbSNP Id: rs1365231553
• gnomAD v2: 19-44280542-C-CTGCAGATGGTTCACCTG
• gnomAD v4: 19-43776390-C-CTGCAGATGGTTCACCTG
• MyVariant Identifiers: chr19:g.44280542_44280543insTGCAGATGGTTCACCTG (hg19) ; chr19:g.43776390_43776391insTGCAGATGGTTCACCTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776390_43776391insTGCAGATGGTTCACCTG , CM000681.2:g.43776390_43776391insTGCAGATGGTTCACCTG	GRCh38
NC_000019.9:g.44280542_44280543insTGCAGATGGTTCACCTG , CM000681.1:g.44280542_44280543insTGCAGATGGTTCACCTG	GRCh37
NC_000019.8:g.48972382_48972383insTGCAGATGGTTCACCTG	NCBI36
NG_052672.1:g.10749_10750insCAGGTGAACCATCTGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+150_255+151insCAGGTGAACCATCTGCA MANE Select	ENSP00000496939.1:n.255+150_255+151insCAGGTGAACCATCTGCA
ENST00000262888.7:c.255+150_255+151insCAGGTGAACCATCTGCA	ENSP00000262888.3:n.255+150_255+151insCAGGTGAACCATCTGCA
ENST00000599107.1:n.286+150_286+151insCAGGTGAACCATCTGCA
ENST00000599720.5:c.160-4288_160-4287insCAGGTGAACCATCTGCA	ENSP00000472513.1:n.160-4288_160-4287insCAGGTGAACCATCTGCA
ENST00000615047.4:c.70+150_70+151insCAGGTGAACCATCTGCA	ENSP00000485014.1:n.70+150_70+151insCAGGTGAACCATCTGCA
NM_002250.2:c.255+150_255+151insCAGGTGAACCATCTGCA	NP_002241.1:n.255+150_255+151insCAGGTGAACCATCTGCA
XM_005258882.2:c.160-1772_160-1771insCAGGTGAACCATCTGCA	XP_005258939.1:n.160-1772_160-1771insCAGGTGAACCATCTGCA
XM_005258883.2:c.70+150_70+151insCAGGTGAACCATCTGCA	XP_005258940.1:n.70+150_70+151insCAGGTGAACCATCTGCA
XM_011526938.1:c.255+150_255+151insCAGGTGAACCATCTGCA	XP_011525240.1:n.255+150_255+151insCAGGTGAACCATCTGCA
XR_935823.1:n.1533+150_1533+151insCAGGTGAACCATCTGCA
XR_002958313.1:n.1533+150_1533+151insCAGGTGAACCATCTGCA
NM_002250.3:c.255+150_255+151insCAGGTGAACCATCTGCA MANE Select	NP_002241.1:n.255+150_255+151insCAGGTGAACCATCTGCA