Canonical Allele Identifier: CA341749238
Gene: AMPD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115220663C>T (hg19) chr1:g.114678042C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114678042C>T , CM000663.2:g.114678042C>T GRCh38
NC_000001.10:g.115220663C>T , CM000663.1:g.115220663C>T GRCh37
NC_000001.9:g.115022186C>T NCBI36
NG_008012.1:g.22514G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.1081-1G>A ENSP00000358551.4:n.1081-1G>A
ENST00000520113.7:c.1093-1G>A MANE Select ENSP00000430075.3:n.1093-1G>A
ENST00000637080.1:c.876-1G>A ENSP00000489753.1:n.876-1G>A
ENST00000639077.1:n.758-1G>A
ENST00000369538.3:c.1180-1G>A ENSP00000358551.3:n.1180-1G>A
ENST00000520113.6:c.1192-1G>A ENSP00000430075.2:n.1192-1G>A
NM_000036.2:c.1192-1G>A NP_000027.2:n.1192-1G>A
NM_001172626.1:c.1180-1G>A NP_001166097.1:n.1180-1G>A
NM_000036.3:c.1093-1G>A MANE Select NP_000027.3:n.1093-1G>A
NM_001172626.2:c.1081-1G>A NP_001166097.2:n.1081-1G>A
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