Canonical Allele Identifier: CA2251974129

Gene: KCNJ12

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.21380986_21380987delinsCT , CM000679.2:g.21380986_21380987delinsCT	GRCh38
NC_000017.10:g.21284298_21284299delinsCT , CM000679.1:g.21284298_21284299delinsCT	GRCh37
NC_000017.9:g.21224891_21224892delinsCT	NCBI36
NG_042809.1:g.9600_9601delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583088.6:c.-179+4073_-179+4074delinsCT MANE Select	ENSP00000463778.1:n.-179+4073_-179+4074delinsCT
ENST00000583088.5:c.-179+4073_-179+4074delinsCT	ENSP00000463778.1:n.-179+4073_-179+4074delinsCT
NM_021012.4:c.-179+4073_-179+4074delinsCT	NP_066292.2:n.-179+4073_-179+4074delinsCT
XM_005256625.3:c.-179+3660_-179+3661delinsCT	XP_005256682.1:n.-179+3660_-179+3661delinsCT
XM_005256625.5:c.-179+3660_-179+3661delinsCT	XP_005256682.1:n.-179+3660_-179+3661delinsCT
NM_021012.5:c.-179+4073_-179+4074delinsCT MANE Select	NP_066292.2:n.-179+4073_-179+4074delinsCT