Canonical Allele Identifier: CA406197888

Gene: KCNN4

Linked Data

• MyVariant Identifiers: chr19:g.44273875T>A (hg19) ; chr19:g.43769723T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769723T>A , CM000681.2:g.43769723T>A	GRCh38
NC_000019.9:g.44273875T>A , CM000681.1:g.44273875T>A	GRCh37
NC_000019.8:g.48965715T>A	NCBI36
NG_052672.1:g.17417A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.548A>T
ENST00000648053.1:n.358A>T
ENST00000648319.1:c.926A>T MANE Select	ENSP00000496939.1:p.Lys309Ile
ENST00000262888.7:c.926A>T	ENSP00000262888.3:p.Lys309Ile
ENST00000598836.1:c.105A>T
ENST00000599720.5:c.*196A>T	ENSP00000472513.1:n.*196A>T
ENST00000600408.1:c.215A>T	ENSP00000472510.1:p.Lys72Ile
ENST00000601549.1:n.235A>T
ENST00000615047.4:c.530A>T	ENSP00000485014.1:p.Lys177Ile
NM_002250.2:c.926A>T	NP_002241.1:p.Lys309Ile
XM_005258882.2:c.830A>T	XP_005258939.1:p.Lys277Ile
XM_005258883.2:c.737A>T	XP_005258940.1:p.Lys246Ile
XR_935823.1:n.2172A>T
XR_002958313.1:n.2318A>T
NM_002250.3:c.926A>T MANE Select	NP_002241.1:p.Lys309Ile