Canonical Allele Identifier: CA2616777262

Gene: KCNJ5

Linked Data

• gnomAD v4: 11-128891749-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128891749T>C , CM000673.2:g.128891749T>C	GRCh38
NC_000011.9:g.128761644T>C , CM000673.1:g.128761644T>C	GRCh37
NC_000011.8:g.128266854T>C	NCBI36
NG_023406.2:g.5332T>C , LRG_333:g.5332T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.-11+28T>C MANE Select	ENSP00000433295.1:n.-11+28T>C
ENST00000338350.4:c.-100+28T>C	ENSP00000339960.4:n.-100+28T>C
ENST00000529694.5:c.-11+28T>C	ENSP00000433295.1:n.-11+28T>C
NM_000890.3:c.-11+28T>C , LRG_333t1:c.-11+28T>C	NP_000881.3:n.-11+28T>C
NM_000890.4:c.-11+28T>C	NP_000881.3:n.-11+28T>C
NM_001354169.1:c.-100+28T>C	NP_001341098.1:n.-100+28T>C
NM_000890.5:c.-11+28T>C MANE Select	NP_000881.3:n.-11+28T>C
NM_001354169.2:c.-100+28T>C	NP_001341098.1:n.-100+28T>C