Canonical Allele Identifier: CA507746433

Gene: KCNN4

Linked Data

• MyVariant Identifiers: chr19:g.44273970G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769818G>A , CM000681.2:g.43769818G>A	GRCh38
NC_000019.9:g.44273970G>A , CM000681.1:g.44273970G>A	GRCh37
NC_000019.8:g.48965810G>A	NCBI36
NG_052672.1:g.17322C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.453C>T
ENST00000648053.1:n.263C>T
ENST00000648319.1:c.831C>T MANE Select	ENSP00000496939.1:p.Cys277=
ENST00000262888.7:c.831C>T	ENSP00000262888.3:p.Cys277=
ENST00000598836.1:c.10C>T
ENST00000599720.5:c.*101C>T	ENSP00000472513.1:n.*101C>T
ENST00000600408.1:c.120C>T	ENSP00000472510.1:p.Cys40=
ENST00000601549.1:n.140C>T
ENST00000615047.4:c.435C>T	ENSP00000485014.1:p.Cys145=
NM_002250.2:c.831C>T	NP_002241.1:p.Cys277=
XM_005258882.2:c.735C>T	XP_005258939.1:p.Cys245=
XM_005258883.2:c.642C>T	XP_005258940.1:p.Cys214=
XR_935823.1:n.2077C>T
XR_002958313.1:n.2223C>T
NM_002250.3:c.831C>T MANE Select	NP_002241.1:p.Cys277=