Canonical Allele Identifier: CA406198800

Gene: KCNN4

Linked Data

• MyVariant Identifiers: chr19:g.44273969T>C (hg19) ; chr19:g.43769817T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769817T>C , CM000681.2:g.43769817T>C	GRCh38
NC_000019.9:g.44273969T>C , CM000681.1:g.44273969T>C	GRCh37
NC_000019.8:g.48965809T>C	NCBI36
NG_052672.1:g.17323A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000601549.2:n.454A>G
ENST00000648053.1:n.264A>G
ENST00000648319.1:c.832A>G MANE Select	ENSP00000496939.1:p.Thr278Ala
ENST00000262888.7:c.832A>G	ENSP00000262888.3:p.Thr278Ala
ENST00000598836.1:c.11A>G
ENST00000599720.5:c.*102A>G	ENSP00000472513.1:n.*102A>G
ENST00000600408.1:c.121A>G	ENSP00000472510.1:p.Thr41Ala
ENST00000601549.1:n.141A>G
ENST00000615047.4:c.436A>G	ENSP00000485014.1:p.Thr146Ala
NM_002250.2:c.832A>G	NP_002241.1:p.Thr278Ala
XM_005258882.2:c.736A>G	XP_005258939.1:p.Thr246Ala
XM_005258883.2:c.643A>G	XP_005258940.1:p.Thr215Ala
XR_935823.1:n.2078A>G
XR_002958313.1:n.2224A>G
NM_002250.3:c.832A>G MANE Select	NP_002241.1:p.Thr278Ala