Canonical Allele Identifier: CA507746432

Gene: KCNN4

Linked Data

• MyVariant Identifiers: chr19:g.44273967T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769815T>A , CM000681.2:g.43769815T>A	GRCh38
NC_000019.9:g.44273967T>A , CM000681.1:g.44273967T>A	GRCh37
NC_000019.8:g.48965807T>A	NCBI36
NG_052672.1:g.17325A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000601549.2:n.456A>T
ENST00000648053.1:n.266A>T
ENST00000648319.1:c.834A>T MANE Select	ENSP00000496939.1:p.Thr278=
ENST00000262888.7:c.834A>T	ENSP00000262888.3:p.Thr278=
ENST00000598836.1:c.13A>T
ENST00000599720.5:c.*104A>T	ENSP00000472513.1:n.*104A>T
ENST00000600408.1:c.123A>T	ENSP00000472510.1:p.Thr41=
ENST00000601549.1:n.143A>T
ENST00000615047.4:c.438A>T	ENSP00000485014.1:p.Thr146=
NM_002250.2:c.834A>T	NP_002241.1:p.Thr278=
XM_005258882.2:c.738A>T	XP_005258939.1:p.Thr246=
XM_005258883.2:c.645A>T	XP_005258940.1:p.Thr215=
XR_935823.1:n.2080A>T
XR_002958313.1:n.2226A>T
NM_002250.3:c.834A>T MANE Select	NP_002241.1:p.Thr278=