Canonical Allele Identifier: CA1581197679

Gene: SLC12A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186662_128186663delinsTG , CM000667.2:g.128186662_128186663delinsTG	GRCh38
NC_000005.9:g.127522354_127522355delinsTG , CM000667.1:g.127522354_127522355delinsTG	GRCh37
NC_000005.8:g.127550253_127550254delinsTG	NCBI36
NG_042286.1:g.107872_107873delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.*31_*32delinsTG MANE Select	ENSP00000262461.2:n.*31_*32delinsTG
ENST00000262461.6:c.*31_*32delinsTG	ENSP00000262461.2:n.*31_*32delinsTG
ENST00000343225.4:c.*31_*32delinsTG	ENSP00000340878.4:n.*31_*32delinsTG
ENST00000509205.5:c.*283_*284delinsTG	ENSP00000427109.1:n.*283_*284delinsTG
NM_001046.2:c.*31_*32delinsTG	NP_001037.1:n.*31_*32delinsTG
NM_001256461.1:c.*31_*32delinsTG	NP_001243390.1:n.*31_*32delinsTG
NR_046207.1:n.3900_3901delinsTG
XM_017009771.1:c.*31_*32delinsTG	XP_016865260.1:n.*31_*32delinsTG
XR_001742214.1:n.3894_3895delinsTG
NM_001046.3:c.*31_*32delinsTG MANE Select	NP_001037.1:n.*31_*32delinsTG
NM_001256461.2:c.*31_*32delinsTG	NP_001243390.1:n.*31_*32delinsTG
NR_046207.2:n.3925_3926delinsTG