Canonical Allele Identifier: CA391614867

Gene: SLC12A6

Linked Data

• MyVariant Identifiers: chr15:g.34553219C>G (hg19) ; chr15:g.34261018C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34261018C>G , CM000677.2:g.34261018C>G	GRCh38
NC_000015.9:g.34553219C>G , CM000677.1:g.34553219C>G	GRCh37
NC_000015.8:g.32340511C>G	NCBI36
NG_007951.1:g.82047G>C , LRG_270:g.82047G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354181.8:c.319G>C MANE Select	ENSP00000346112.3:p.Asp107His
ENST00000675289.1:n.1101G>C
ENST00000676379.1:c.319G>C	ENSP00000502539.1:p.Asp107His
ENST00000290209.9:c.166G>C	ENSP00000290209.5:p.Asp56His
ENST00000354181.7:c.319G>C	ENSP00000346112.3:p.Asp107His
ENST00000397702.6:c.142G>C	ENSP00000380814.2:p.Asp48His
ENST00000397707.6:c.274G>C	ENSP00000380819.2:p.Asp92His
ENST00000458406.6:c.142G>C	ENSP00000387725.2:p.Asp48His
ENST00000558589.5:c.292G>C	ENSP00000452776.1:p.Asp98His
ENST00000558667.5:c.319G>C	ENSP00000453473.1:p.Asp107His
ENST00000559236.5:c.319G>C	ENSP00000452828.1:p.Asp107His
ENST00000559484.1:c.142G>C	ENSP00000452857.1:p.Asp48His
ENST00000559523.5:c.142G>C	ENSP00000452904.1:p.Asp48His
ENST00000559664.5:c.319G>C	ENSP00000453702.1:p.Asp107His
ENST00000560164.5:c.-99G>C	ENSP00000452705.1:n.-99G>C
ENST00000560332.1:c.-99G>C	ENSP00000454037.1:n.-99G>C
ENST00000560611.5:c.319G>C	ENSP00000454168.1:p.Asp107His
ENST00000561080.5:c.319G>C	ENSP00000454069.1:p.Asp107His
ENST00000561120.5:c.292G>C	ENSP00000452771.1:p.Asp98His
NM_001042494.1:c.142G>C	NP_001035959.1:p.Asp48His
NM_001042495.1:c.142G>C	NP_001035960.1:p.Asp48His
NM_001042496.1:c.292G>C	NP_001035961.1:p.Asp98His
NM_001042497.1:c.274G>C	NP_001035962.1:p.Asp92His
NM_005135.2:c.166G>C , LRG_270t1:c.166G>C	NP_005126.1:p.Asp56His
NM_133647.1:c.319G>C , LRG_270t2:c.319G>C	NP_598408.1:p.Asp107His
XM_006720793.2:c.319G>C	XP_006720856.1:p.Asp107His
XM_011522267.1:c.319G>C	XP_011520569.1:p.Asp107His
XM_011522268.1:c.319G>C	XP_011520570.1:p.Asp107His
XM_011522269.1:c.319G>C	XP_011520571.1:p.Asp107His
XR_429476.2:n.325G>C
XR_931960.1:n.325G>C
XR_931961.1:n.325G>C
NM_001365088.1:c.319G>C MANE Select	NP_001352017.1:p.Asp107His
XM_006720793.4:c.319G>C	XP_006720856.1:p.Asp107His
XM_011522269.3:c.319G>C	XP_011520571.1:p.Asp107His
XR_931960.3:n.1569G>C
NM_001042494.2:c.142G>C	NP_001035959.1:p.Asp48His
NM_001042495.2:c.142G>C	NP_001035960.1:p.Asp48His
NM_001042496.2:c.292G>C	NP_001035961.1:p.Asp98His
NM_001042497.2:c.274G>C	NP_001035962.1:p.Asp92His
NM_133647.2:c.319G>C	NP_598408.1:p.Asp107His