Canonical Allele Identifier: CA721944493

Gene: SLC12A3

Linked Data

• dbSNP Id: rs1192366378
• gnomAD v3: 16-56894711-TC-T
• gnomAD v4: 16-56894711-TC-T
• MyVariant Identifiers: chr16:g.56928624del (hg19) ; chr16:g.56894712del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56894715del , CM000678.2:g.56894715del	GRCh38
NC_000016.9:g.56928627del , CM000678.1:g.56928627del	GRCh37
NC_000016.8:g.55486128del	NCBI36
NG_009386.1:g.34509del
NG_009386.2:g.34509del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.2633+73del MANE Select	ENSP00000456149.2:n.2633+73del
ENST00000262502.5:c.2630+73del	ENSP00000262502.5:n.2630+73del
ENST00000438926.6:c.2660+73del	ENSP00000402152.2:n.2660+73del
ENST00000563236.5:c.2633+73del	ENSP00000456149.1:n.2633+73del
ENST00000566786.5:c.2657+73del	ENSP00000457552.1:n.2657+73del
NM_000339.2:c.2660+73del	NP_000330.2:n.2660+73del
NM_001126107.1:c.2657+73del	NP_001119579.1:n.2657+73del
NM_001126108.1:c.2633+73del	NP_001119580.1:n.2633+73del
XM_005256119.1:c.2630+73del	XP_005256176.1:n.2630+73del
XM_005256119.2:c.2630+73del	XP_005256176.1:n.2630+73del
NM_000339.3:c.2660+73del	NP_000330.3:n.2660+73del
NM_001126107.2:c.2657+73del	NP_001119579.2:n.2657+73del
NM_001126108.2:c.2633+73del MANE Select	NP_001119580.2:n.2633+73del