Canonical Allele Identifier: CA569615080
Gene: SLC16A10 HGNC NCBI

Linked Data

dbSNP Id: rs1177889363
gnomAD v2: 6-111544168-G-A
gnomAD v3: 6-111222965-G-A
gnomAD v4: 6-111222965-G-A
MyVariant Identifiers: chr6:g.111544168G>A (hg19) chr6:g.111222965G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222965G>A , CM000668.2:g.111222965G>A GRCh38
NC_000006.11:g.111544168G>A , CM000668.1:g.111544168G>A GRCh37
NC_000006.10:g.111650861G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*730G>A MANE Select ENSP00000357844.4:n.*730G>A
ENST00000368850.4:c.*730G>A ENSP00000357843.1:n.*730G>A
ENST00000368851.9:c.*730G>A ENSP00000357844.4:n.*730G>A
NM_018593.4:c.*730G>A NP_061063.2:n.*730G>A
XM_005266818.2:c.*684G>A XP_005266875.1:n.*684G>A
XM_017010237.1:c.*730G>A XP_016865726.1:n.*730G>A
XR_001743158.1:n.2560G>A
NM_018593.5:c.*730G>A MANE Select NP_061063.2:n.*730G>A
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