Canonical Allele Identifier: CA489410662

Gene: SLC12A6

Linked Data

• MyVariant Identifiers: chr15:g.34528224G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34236023G>A , CM000677.2:g.34236023G>A	GRCh38
NC_000015.9:g.34528224G>A , CM000677.1:g.34528224G>A	GRCh37
NC_000015.8:g.32315516G>A	NCBI36
NG_007951.1:g.107042C>T , LRG_270:g.107042C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354181.8:c.3219C>T MANE Select	ENSP00000346112.3:p.Asn1073=
ENST00000676379.1:c.3219C>T	ENSP00000502539.1:p.Asn1073=
ENST00000290209.9:c.3066C>T	ENSP00000290209.5:p.Asn1022=
ENST00000354181.7:c.3219C>T	ENSP00000346112.3:p.Asn1073=
ENST00000397702.6:c.3042C>T	ENSP00000380814.2:p.Asn1014=
ENST00000397707.6:c.3174C>T	ENSP00000380819.2:p.Asn1058=
ENST00000458406.6:c.3042C>T	ENSP00000387725.2:p.Asn1014=
ENST00000558589.5:c.3192C>T	ENSP00000452776.1:p.Asn1064=
ENST00000558667.5:c.3219C>T	ENSP00000453473.1:p.Asn1073=
ENST00000559523.5:c.*242C>T	ENSP00000452904.1:n.*242C>T
ENST00000559664.5:c.*428C>T	ENSP00000453702.1:n.*428C>T
ENST00000560164.5:c.2655C>T	ENSP00000452705.1:p.Asn885=
ENST00000560611.5:c.3219C>T	ENSP00000454168.1:p.Asn1073=
ENST00000561080.5:c.*457C>T	ENSP00000454069.1:n.*457C>T
NM_001042494.1:c.3042C>T	NP_001035959.1:p.Asn1014=
NM_001042495.1:c.3042C>T	NP_001035960.1:p.Asn1014=
NM_001042496.1:c.3192C>T	NP_001035961.1:p.Asn1064=
NM_001042497.1:c.3174C>T	NP_001035962.1:p.Asn1058=
NM_005135.2:c.3066C>T , LRG_270t1:c.3066C>T	NP_005126.1:p.Asn1022=
NM_133647.1:c.3219C>T , LRG_270t2:c.3219C>T	NP_598408.1:p.Asn1073=
XM_006720793.2:c.3072C>T	XP_006720856.1:p.Asn1024=
XM_011522267.1:c.3219C>T	XP_011520569.1:p.Asn1073=
XM_011522268.1:c.3219C>T	XP_011520570.1:p.Asn1073=
XR_429476.2:n.3225C>T
NM_001365088.1:c.3219C>T MANE Select	NP_001352017.1:p.Asn1073=
XM_006720793.4:c.3072C>T	XP_006720856.1:p.Asn1024=
XR_931960.3:n.4498C>T
NM_001042494.2:c.3042C>T	NP_001035959.1:p.Asn1014=
NM_001042495.2:c.3042C>T	NP_001035960.1:p.Asn1014=
NM_001042496.2:c.3192C>T	NP_001035961.1:p.Asn1064=
NM_001042497.2:c.3174C>T	NP_001035962.1:p.Asn1058=
NM_133647.2:c.3219C>T	NP_598408.1:p.Asn1073=