Canonical Allele Identifier: CA406198087

Gene: KCNN4

Linked Data

• MyVariant Identifiers: chr19:g.44273893A>G (hg19) ; chr19:g.43769741A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769741A>G , CM000681.2:g.43769741A>G	GRCh38
NC_000019.9:g.44273893A>G , CM000681.1:g.44273893A>G	GRCh37
NC_000019.8:g.48965733A>G	NCBI36
NG_052672.1:g.17399T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.530T>C
ENST00000648053.1:n.340T>C
ENST00000648319.1:c.908T>C MANE Select	ENSP00000496939.1:p.Met303Thr
ENST00000262888.7:c.908T>C	ENSP00000262888.3:p.Met303Thr
ENST00000598836.1:c.87T>C
ENST00000599720.5:c.*178T>C	ENSP00000472513.1:n.*178T>C
ENST00000600408.1:c.197T>C	ENSP00000472510.1:p.Met66Thr
ENST00000601549.1:n.217T>C
ENST00000615047.4:c.512T>C	ENSP00000485014.1:p.Met171Thr
NM_002250.2:c.908T>C	NP_002241.1:p.Met303Thr
XM_005258882.2:c.812T>C	XP_005258939.1:p.Met271Thr
XM_005258883.2:c.719T>C	XP_005258940.1:p.Met240Thr
XR_935823.1:n.2154T>C
XR_002958313.1:n.2300T>C
NM_002250.3:c.908T>C MANE Select	NP_002241.1:p.Met303Thr