Canonical Allele Identifier: CA2838775550

Gene: SLC12A3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56904203A>T , CM000678.2:g.56904203A>T	GRCh38
NC_000016.9:g.56938115A>T , CM000678.1:g.56938115A>T	GRCh37
NC_000016.8:g.55495616A>T	NCBI36
NG_009386.1:g.43997A>T
NG_009386.2:g.43997A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.2857-192A>T MANE Select	ENSP00000456149.2:n.2857-192A>T
ENST00000262502.5:c.2854-192A>T	ENSP00000262502.5:n.2854-192A>T
ENST00000438926.6:c.2884-192A>T	ENSP00000402152.2:n.2884-192A>T
ENST00000563236.5:c.2857-192A>T	ENSP00000456149.1:n.2857-192A>T
ENST00000566786.5:c.2881-192A>T	ENSP00000457552.1:n.2881-192A>T
ENST00000569002.1:n.288-192A>T
NM_000339.2:c.2884-192A>T	NP_000330.2:n.2884-192A>T
NM_001126107.1:c.2881-192A>T	NP_001119579.1:n.2881-192A>T
NM_001126108.1:c.2857-192A>T	NP_001119580.1:n.2857-192A>T
XM_005256119.1:c.2854-192A>T	XP_005256176.1:n.2854-192A>T
XM_005256119.2:c.2854-192A>T	XP_005256176.1:n.2854-192A>T
NM_000339.3:c.2884-192A>T	NP_000330.3:n.2884-192A>T
NM_001126107.2:c.2881-192A>T	NP_001119579.2:n.2881-192A>T
NM_001126108.2:c.2857-192A>T MANE Select	NP_001119580.2:n.2857-192A>T