Canonical Allele Identifier: CA406198843

Gene: KCNN4

Linked Data

• MyVariant Identifiers: chr19:g.44273972A>T (hg19) ; chr19:g.43769820A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769820A>T , CM000681.2:g.43769820A>T	GRCh38
NC_000019.9:g.44273972A>T , CM000681.1:g.44273972A>T	GRCh37
NC_000019.8:g.48965812A>T	NCBI36
NG_052672.1:g.17320T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.451T>A
ENST00000648053.1:n.261T>A
ENST00000648319.1:c.829T>A MANE Select	ENSP00000496939.1:p.Cys277Ser
ENST00000262888.7:c.829T>A	ENSP00000262888.3:p.Cys277Ser
ENST00000598836.1:c.8T>A
ENST00000599720.5:c.*99T>A	ENSP00000472513.1:n.*99T>A
ENST00000600408.1:c.118T>A	ENSP00000472510.1:p.Cys40Ser
ENST00000601549.1:n.138T>A
ENST00000615047.4:c.433T>A	ENSP00000485014.1:p.Cys145Ser
NM_002250.2:c.829T>A	NP_002241.1:p.Cys277Ser
XM_005258882.2:c.733T>A	XP_005258939.1:p.Cys245Ser
XM_005258883.2:c.640T>A	XP_005258940.1:p.Cys214Ser
XR_935823.1:n.2075T>A
XR_002958313.1:n.2221T>A
NM_002250.3:c.829T>A MANE Select	NP_002241.1:p.Cys277Ser