Canonical Allele Identifier: CA682765722
Gene: GNPTAB HGNC NCBI

Linked Data

dbSNP Id: rs1193234774
MyVariant Identifiers: chr12:g.102224485A>T (hg19) chr12:g.101830707A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101830707A>T , CM000674.2:g.101830707A>T GRCh38
NC_000012.11:g.102224485A>T , CM000674.1:g.102224485A>T GRCh37
NC_000012.10:g.100748616A>T NCBI36
NG_021243.1:g.5161T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.-32T>A MANE Select ENSP00000299314.7:n.-32T>A
ENST00000299314.11:c.-32T>A ENSP00000299314.7:n.-32T>A
ENST00000392919.4:c.-32T>A ENSP00000376651.4:n.-32T>A
ENST00000549940.5:c.-32T>A ENSP00000449150.1:n.-32T>A
NM_024312.4:c.-32T>A NP_077288.2:n.-32T>A
XM_006719593.2:c.-32T>A XP_006719656.1:n.-32T>A
XM_006719593.3:c.-32T>A XP_006719656.1:n.-32T>A
XM_017019961.1:c.-181T>A XP_016875450.1:n.-181T>A
XM_017019962.2:c.-1382T>A XP_016875451.1:n.-1382T>A
NM_024312.5:c.-32T>A MANE Select NP_077288.2:n.-32T>A
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