Canonical Allele Identifier: CA391618470
Gene: SLC12A6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34237457G>T , CM000677.2:g.34237457G>T GRCh38
NC_000015.9:g.34529658G>T , CM000677.1:g.34529658G>T GRCh37
NC_000015.8:g.32316950G>T NCBI36
NG_007951.1:g.105608C>A , LRG_270:g.105608C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000354181.8:c.2896C>A MANE Select ENSP00000346112.3:p.His966Asn
ENST00000676379.1:c.2896C>A ENSP00000502539.1:p.His966Asn
ENST00000290209.9:c.2743C>A ENSP00000290209.5:p.His915Asn
ENST00000354181.7:c.2896C>A ENSP00000346112.3:p.His966Asn
ENST00000397702.6:c.2719C>A ENSP00000380814.2:p.His907Asn
ENST00000397707.6:c.2851C>A ENSP00000380819.2:p.His951Asn
ENST00000458406.6:c.2719C>A ENSP00000387725.2:p.His907Asn
ENST00000558589.5:c.2869C>A ENSP00000452776.1:p.His957Asn
ENST00000558667.5:c.2896C>A ENSP00000453473.1:p.His966Asn
ENST00000559076.1:n.259C>A
ENST00000559523.5:c.2719C>A ENSP00000452904.1:p.His907Asn
ENST00000559664.5:c.*105C>A ENSP00000453702.1:n.*105C>A
ENST00000560164.5:c.2332C>A ENSP00000452705.1:p.His778Asn
ENST00000560611.5:c.2896C>A ENSP00000454168.1:p.His966Asn
ENST00000561080.5:c.*105C>A ENSP00000454069.1:n.*105C>A
NM_001042494.1:c.2719C>A NP_001035959.1:p.His907Asn
NM_001042495.1:c.2719C>A NP_001035960.1:p.His907Asn
NM_001042496.1:c.2869C>A NP_001035961.1:p.His957Asn
NM_001042497.1:c.2851C>A NP_001035962.1:p.His951Asn
NM_005135.2:c.2743C>A , LRG_270t1:c.2743C>A NP_005126.1:p.His915Asn
NM_133647.1:c.2896C>A , LRG_270t2:c.2896C>A NP_598408.1:p.His966Asn
XM_006720793.2:c.2749C>A XP_006720856.1:p.His917Asn
XM_011522267.1:c.2896C>A XP_011520569.1:p.His966Asn
XM_011522268.1:c.2896C>A XP_011520570.1:p.His966Asn
XR_429476.2:n.2902C>A
XR_931960.1:n.2902C>A
NM_001365088.1:c.2896C>A MANE Select NP_001352017.1:p.His966Asn
XM_006720793.4:c.2749C>A XP_006720856.1:p.His917Asn
XR_931960.3:n.4146C>A
NM_001042494.2:c.2719C>A NP_001035959.1:p.His907Asn
NM_001042495.2:c.2719C>A NP_001035960.1:p.His907Asn
NM_001042496.2:c.2869C>A NP_001035961.1:p.His957Asn
NM_001042497.2:c.2851C>A NP_001035962.1:p.His951Asn
NM_133647.2:c.2896C>A NP_598408.1:p.His966Asn