Canonical Allele Identifier: CA391617432

Gene: SLC12A6

Linked Data

• MyVariant Identifiers: chr15:g.34528217G>T (hg19) ; chr15:g.34236016G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34236016G>T , CM000677.2:g.34236016G>T	GRCh38
NC_000015.9:g.34528217G>T , CM000677.1:g.34528217G>T	GRCh37
NC_000015.8:g.32315509G>T	NCBI36
NG_007951.1:g.107049C>A , LRG_270:g.107049C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354181.8:c.3226C>A MANE Select	ENSP00000346112.3:p.Pro1076Thr
ENST00000676379.1:c.3226C>A	ENSP00000502539.1:p.Pro1076Thr
ENST00000290209.9:c.3073C>A	ENSP00000290209.5:p.Pro1025Thr
ENST00000354181.7:c.3226C>A	ENSP00000346112.3:p.Pro1076Thr
ENST00000397702.6:c.3049C>A	ENSP00000380814.2:p.Pro1017Thr
ENST00000397707.6:c.3181C>A	ENSP00000380819.2:p.Pro1061Thr
ENST00000458406.6:c.3049C>A	ENSP00000387725.2:p.Pro1017Thr
ENST00000558589.5:c.3199C>A	ENSP00000452776.1:p.Pro1067Thr
ENST00000558667.5:c.3226C>A	ENSP00000453473.1:p.Pro1076Thr
ENST00000559523.5:c.*249C>A	ENSP00000452904.1:n.*249C>A
ENST00000559664.5:c.*435C>A	ENSP00000453702.1:n.*435C>A
ENST00000560164.5:c.2662C>A	ENSP00000452705.1:p.Pro888Thr
ENST00000560611.5:c.3226C>A	ENSP00000454168.1:p.Pro1076Thr
ENST00000561080.5:c.*464C>A	ENSP00000454069.1:n.*464C>A
NM_001042494.1:c.3049C>A	NP_001035959.1:p.Pro1017Thr
NM_001042495.1:c.3049C>A	NP_001035960.1:p.Pro1017Thr
NM_001042496.1:c.3199C>A	NP_001035961.1:p.Pro1067Thr
NM_001042497.1:c.3181C>A	NP_001035962.1:p.Pro1061Thr
NM_005135.2:c.3073C>A , LRG_270t1:c.3073C>A	NP_005126.1:p.Pro1025Thr
NM_133647.1:c.3226C>A , LRG_270t2:c.3226C>A	NP_598408.1:p.Pro1076Thr
XM_006720793.2:c.3079C>A	XP_006720856.1:p.Pro1027Thr
XM_011522267.1:c.3226C>A	XP_011520569.1:p.Pro1076Thr
XM_011522268.1:c.3226C>A	XP_011520570.1:p.Pro1076Thr
XR_429476.2:n.3232C>A
NM_001365088.1:c.3226C>A MANE Select	NP_001352017.1:p.Pro1076Thr
XM_006720793.4:c.3079C>A	XP_006720856.1:p.Pro1027Thr
XR_931960.3:n.4505C>A
NM_001042494.2:c.3049C>A	NP_001035959.1:p.Pro1017Thr
NM_001042495.2:c.3049C>A	NP_001035960.1:p.Pro1017Thr
NM_001042496.2:c.3199C>A	NP_001035961.1:p.Pro1067Thr
NM_001042497.2:c.3181C>A	NP_001035962.1:p.Pro1061Thr
NM_133647.2:c.3226C>A	NP_598408.1:p.Pro1076Thr