Canonical Allele Identifier: CA1654828623
Gene: SLC16A10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222988A= , CM000668.2:g.111222988A= GRCh38
NC_000006.11:g.111544191A= , CM000668.1:g.111544191A= GRCh37
NC_000006.10:g.111650884A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*753A= MANE Select ENSP00000357844.4:n.*753A=
ENST00000368850.4:c.*753A= ENSP00000357843.1:n.*753A=
ENST00000368851.9:c.*753A= ENSP00000357844.4:n.*753A=
NM_018593.4:c.*753A= NP_061063.2:n.*753A=
XM_005266818.2:c.*707A= XP_005266875.1:n.*707A=
XM_017010237.1:c.*753A= XP_016865726.1:n.*753A=
XR_001743158.1:n.2583A=
NM_018593.5:c.*753A= MANE Select NP_061063.2:n.*753A=