Canonical Allele Identifier: CA446302736

Gene: SLC12A2

Linked Data

• MyVariant Identifiers: chr5:g.127522251T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186559T>G , CM000667.2:g.128186559T>G	GRCh38
NC_000005.9:g.127522251T>G , CM000667.1:g.127522251T>G	GRCh37
NC_000005.8:g.127550150T>G	NCBI36
NG_042286.1:g.107769T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.3567T>G MANE Select	ENSP00000262461.2:p.Ala1189=
ENST00000262461.6:c.3567T>G	ENSP00000262461.2:p.Ala1189=
ENST00000343225.4:c.3519T>G	ENSP00000340878.4:p.Ala1173=
ENST00000509205.5:c.*180T>G	ENSP00000427109.1:n.*180T>G
NM_001046.2:c.3567T>G	NP_001037.1:p.Ala1189=
NM_001256461.1:c.3519T>G	NP_001243390.1:p.Ala1173=
NR_046207.1:n.3797T>G
XM_017009771.1:c.1809T>G	XP_016865260.1:p.Ala603=
XR_001742214.1:n.3791T>G
NM_001046.3:c.3567T>G MANE Select	NP_001037.1:p.Ala1189=
NM_001256461.2:c.3519T>G	NP_001243390.1:p.Ala1173=
NR_046207.2:n.3822T>G