Canonical Allele Identifier: CA3212250289

Gene: SLC12A6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34236022T= , CM000677.2:g.34236022T=	GRCh38
NC_000015.9:g.34528223T= , CM000677.1:g.34528223T=	GRCh37
NC_000015.8:g.32315515T=	NCBI36
NG_007951.1:g.107043A= , LRG_270:g.107043A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001365088.1:c.3220A= MANE Select	NP_001352017.1:p.Met1074=
ENST00000354181.8:c.3220A= MANE Select	ENSP00000346112.3:p.Met1074=
NM_001042494.1:c.3043A=	NP_001035959.1:p.Met1015=
NM_001042494.2:c.3043A=	NP_001035959.1:p.Met1015=
NM_001042495.1:c.3043A=	NP_001035960.1:p.Met1015=
NM_001042495.2:c.3043A=	NP_001035960.1:p.Met1015=
NM_001042496.1:c.3193A=	NP_001035961.1:p.Met1065=
NM_001042496.2:c.3193A=	NP_001035961.1:p.Met1065=
NM_001042497.1:c.3175A=	NP_001035962.1:p.Met1059=
NM_001042497.2:c.3175A=	NP_001035962.1:p.Met1059=
NM_005135.2:c.3067A= , LRG_270t1:c.3067A=	NP_005126.1:p.Met1023=
NM_133647.1:c.3220A= , LRG_270t2:c.3220A=	NP_598408.1:p.Met1074=
NM_133647.2:c.3220A=	NP_598408.1:p.Met1074=
ENST00000290209.9:c.3067A=	ENSP00000290209.5:p.Met1023=
ENST00000354181.7:c.3220A=	ENSP00000346112.3:p.Met1074=
ENST00000397702.6:c.3043A=	ENSP00000380814.2:p.Met1015=
ENST00000397707.6:c.3175A=	ENSP00000380819.2:p.Met1059=
ENST00000458406.6:c.3043A=	ENSP00000387725.2:p.Met1015=
ENST00000558589.5:c.3193A=	ENSP00000452776.1:p.Met1065=
ENST00000558667.5:c.3220A=	ENSP00000453473.1:p.Met1074=
ENST00000559523.5:c.*243A=	ENSP00000452904.1:n.*243A=
ENST00000559664.5:c.*429A=	ENSP00000453702.1:n.*429A=
ENST00000560164.5:c.2656A=	ENSP00000452705.1:p.Met886=
ENST00000560611.5:c.3220A=	ENSP00000454168.1:p.Met1074=
ENST00000561080.5:c.*458A=	ENSP00000454069.1:n.*458A=
ENST00000676379.1:c.3220A=	ENSP00000502539.1:p.Met1074=
XM_006720793.2:c.3073A=	XP_006720856.1:p.Met1025=
XM_006720793.4:c.3073A=	XP_006720856.1:p.Met1025=
XM_011522267.1:c.3220A=	XP_011520569.1:p.Met1074=
XM_011522268.1:c.3220A=	XP_011520570.1:p.Met1074=
XR_429476.2:n.3226A=
XR_931960.3:n.4499A=