Canonical Allele Identifier: CA383249037

Gene: KCNJ5

Linked Data

• gnomAD v4: 11-128911830-T-C
• MyVariant Identifiers: chr11:g.128781725T>C (hg19) ; chr11:g.128911830T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128911830T>C , CM000673.2:g.128911830T>C	GRCh38
NC_000011.9:g.128781725T>C , CM000673.1:g.128781725T>C	GRCh37
NC_000011.8:g.128286935T>C	NCBI36
NG_023406.2:g.25413T>C , LRG_333:g.25413T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529694.6:c.557T>C MANE Select	ENSP00000433295.1:p.Met186Thr
ENST00000338350.4:c.557T>C	ENSP00000339960.4:p.Met186Thr
ENST00000529694.5:c.557T>C	ENSP00000433295.1:p.Met186Thr
ENST00000533599.1:c.557T>C	ENSP00000434266.1:p.Met186Thr
NM_000890.3:c.557T>C , LRG_333t1:c.557T>C	NP_000881.3:p.Met186Thr
XM_011542809.1:c.557T>C	XP_011541111.1:p.Met186Thr
XM_011542810.1:c.557T>C	XP_011541112.1:p.Met186Thr
NM_000890.4:c.557T>C	NP_000881.3:p.Met186Thr
NM_001354169.1:c.557T>C	NP_001341098.1:p.Met186Thr
XM_011542809.2:c.557T>C	XP_011541111.1:p.Met186Thr
XM_011542810.3:c.557T>C	XP_011541112.1:p.Met186Thr
NM_000890.5:c.557T>C MANE Select	NP_000881.3:p.Met186Thr
NM_001354169.2:c.557T>C	NP_001341098.1:p.Met186Thr