Canonical Allele Identifier: CA406198419

Gene: KCNN4

Linked Data

• MyVariant Identifiers: chr19:g.44273925G>T (hg19) ; chr19:g.43769773G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769773G>T , CM000681.2:g.43769773G>T	GRCh38
NC_000019.9:g.44273925G>T , CM000681.1:g.44273925G>T	GRCh37
NC_000019.8:g.48965765G>T	NCBI36
NG_052672.1:g.17367C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.498C>A
ENST00000648053.1:n.308C>A
ENST00000648319.1:c.876C>A MANE Select	ENSP00000496939.1:p.Asn292Lys
ENST00000262888.7:c.876C>A	ENSP00000262888.3:p.Asn292Lys
ENST00000598836.1:c.55C>A
ENST00000599720.5:c.*146C>A	ENSP00000472513.1:n.*146C>A
ENST00000600408.1:c.165C>A	ENSP00000472510.1:p.Asn55Lys
ENST00000601549.1:n.185C>A
ENST00000615047.4:c.480C>A	ENSP00000485014.1:p.Asn160Lys
NM_002250.2:c.876C>A	NP_002241.1:p.Asn292Lys
XM_005258882.2:c.780C>A	XP_005258939.1:p.Asn260Lys
XM_005258883.2:c.687C>A	XP_005258940.1:p.Asn229Lys
XR_935823.1:n.2122C>A
XR_002958313.1:n.2268C>A
NM_002250.3:c.876C>A MANE Select	NP_002241.1:p.Asn292Lys