Canonical Allele Identifier: CA2614199798
Gene: PYGM HGNC NCBI

Linked Data

gnomAD v4: 11-64747580-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64747580A>T , CM000673.2:g.64747580A>T GRCh38
NC_000011.9:g.64515052A>T , CM000673.1:g.64515052A>T GRCh37
NC_000011.8:g.64271628A>T NCBI36
NG_007574.1:g.2877T>A , LRG_100:g.2877T>A
NG_013018.1:g.18136T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.2178-222T>A MANE Select ENSP00000164139.3:n.2178-222T>A
ENST00000164139.3:c.2178-222T>A ENSP00000164139.3:n.2178-222T>A
ENST00000377432.7:c.1914-222T>A ENSP00000366650.3:n.1914-222T>A
ENST00000483742.1:n.1309T>A
NM_001164716.1:c.1914-222T>A NP_001158188.1:n.1914-222T>A
NM_005609.2:c.2178-222T>A NP_005600.1:n.2178-222T>A
NM_005609.3:c.2178-222T>A NP_005600.1:n.2178-222T>A
NM_005609.4:c.2178-222T>A MANE Select NP_005600.1:n.2178-222T>A
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