Canonical Allele Identifier: CA1574344772

Gene: KCNN2

Linked Data

• dbSNP Id: rs1761285632

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.114463200T>G , CM000667.2:g.114463200T>G	GRCh38
NC_000005.9:g.113798897T>G , CM000667.1:g.113798897T>G	GRCh37
NC_000005.8:g.113826796T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000512097.10:c.1977+10T>G	ENSP00000427120.4:n.1977+10T>G
ENST00000512097.9:c.1977+10T>G	ENSP00000427120.4:n.1977+10T>G
ENST00000631899.2:c.1181+10T>G
ENST00000673685.1:c.1779+10T>G MANE Select	ENSP00000501239.1:n.1779+10T>G
ENST00000264773.7:c.1143+10T>G	ENSP00000264773.2:n.1143+10T>G
ENST00000503706.5:c.99+10T>G	ENSP00000421439.1:n.99+10T>G
ENST00000505491.1:c.99+10T>G	ENSP00000421095.1:n.99+10T>G
ENST00000507750.5:n.393+10T>G
ENST00000512097.7:c.1143+10T>G	ENSP00000427120.3:n.1143+10T>G
ENST00000610748.4:c.99+10T>G	ENSP00000483124.1:n.99+10T>G
ENST00000631899.1:c.1143+10T>G	ENSP00000487849.1:n.1143+10T>G
NM_001278204.1:c.99+10T>G	NP_001265133.1:n.99+10T>G
NM_021614.3:c.1143+10T>G	NP_067627.2:n.1143+10T>G
NM_170775.2:c.99+10T>G	NP_740721.1:n.99+10T>G
NR_103458.1:n.542+10T>G
NR_130785.1:n.1539+6562A>C
XM_011543387.1:c.1977+10T>G	XP_011541689.1:n.1977+10T>G
XM_011543388.1:c.1977+10T>G	XP_011541690.1:n.1977+10T>G
XM_011543389.1:c.1977+10T>G	XP_011541691.1:n.1977+10T>G
XM_017009457.1:c.231+10T>G	XP_016864946.1:n.231+10T>G
NM_001372233.1:c.1977+10T>G	NP_001359162.1:n.1977+10T>G
NM_021614.4:c.1779+10T>G MANE Select	NP_067627.3:n.1779+10T>G
NM_170775.3:c.99+10T>G	NP_740721.1:n.99+10T>G
NR_103458.2:n.561+10T>G
NM_001278204.2:c.99+10T>G	NP_001265133.1:n.99+10T>G
NR_174097.1:n.1430+10T>G