Canonical Allele Identifier: CA489408379

Gene: SLC12A6

Linked Data

• MyVariant Identifiers: chr15:g.34549870A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34257669A>G , CM000677.2:g.34257669A>G	GRCh38
NC_000015.9:g.34549870A>G , CM000677.1:g.34549870A>G	GRCh37
NC_000015.8:g.32337162A>G	NCBI36
NG_007951.1:g.85396T>C , LRG_270:g.85396T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354181.8:c.663T>C MANE Select	ENSP00000346112.3:p.Phe221=
ENST00000675289.1:n.1445T>C
ENST00000676379.1:c.663T>C	ENSP00000502539.1:p.Phe221=
ENST00000290209.9:c.510T>C	ENSP00000290209.5:p.Phe170=
ENST00000354181.7:c.663T>C	ENSP00000346112.3:p.Phe221=
ENST00000397702.6:c.486T>C	ENSP00000380814.2:p.Phe162=
ENST00000397707.6:c.618T>C	ENSP00000380819.2:p.Phe206=
ENST00000458406.6:c.486T>C	ENSP00000387725.2:p.Phe162=
ENST00000558589.5:c.636T>C	ENSP00000452776.1:p.Phe212=
ENST00000558667.5:c.663T>C	ENSP00000453473.1:p.Phe221=
ENST00000559523.5:c.486T>C	ENSP00000452904.1:p.Phe162=
ENST00000559664.5:c.663T>C	ENSP00000453702.1:p.Phe221=
ENST00000560164.5:c.126+1144T>C	ENSP00000452705.1:n.126+1144T>C
ENST00000560332.1:c.246T>C	ENSP00000454037.1:p.Phe82=
ENST00000560611.5:c.663T>C	ENSP00000454168.1:p.Phe221=
ENST00000561080.5:c.663T>C	ENSP00000454069.1:p.Phe221=
NM_001042494.1:c.486T>C	NP_001035959.1:p.Phe162=
NM_001042495.1:c.486T>C	NP_001035960.1:p.Phe162=
NM_001042496.1:c.636T>C	NP_001035961.1:p.Phe212=
NM_001042497.1:c.618T>C	NP_001035962.1:p.Phe206=
NM_005135.2:c.510T>C , LRG_270t1:c.510T>C	NP_005126.1:p.Phe170=
NM_133647.1:c.663T>C , LRG_270t2:c.663T>C	NP_598408.1:p.Phe221=
XM_006720793.2:c.543+1144T>C	XP_006720856.1:n.543+1144T>C
XM_011522267.1:c.663T>C	XP_011520569.1:p.Phe221=
XM_011522268.1:c.663T>C	XP_011520570.1:p.Phe221=
XM_011522269.1:c.663T>C	XP_011520571.1:p.Phe221=
XR_429476.2:n.669T>C
XR_931960.1:n.669T>C
XR_931961.1:n.669T>C
NM_001365088.1:c.663T>C MANE Select	NP_001352017.1:p.Phe221=
XM_006720793.4:c.543+1144T>C	XP_006720856.1:n.543+1144T>C
XM_011522269.3:c.663T>C	XP_011520571.1:p.Phe221=
XR_931960.3:n.1913T>C
NM_001042494.2:c.486T>C	NP_001035959.1:p.Phe162=
NM_001042495.2:c.486T>C	NP_001035960.1:p.Phe162=
NM_001042496.2:c.636T>C	NP_001035961.1:p.Phe212=
NM_001042497.2:c.618T>C	NP_001035962.1:p.Phe206=
NM_133647.2:c.663T>C	NP_598408.1:p.Phe221=