Canonical Allele Identifier: CA16607274
Gene: ALDOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30053445C>T , CM000678.2:g.30053445C>T GRCh38
NC_000016.9:g.30064766C>T , CM000678.1:g.30064766C>T GRCh37
NC_000016.8:g.29972267C>T NCBI36
NG_008010.1:g.5276C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338110.11:c.-30-19C>T ENSP00000336927.6:n.-30-19C>T
ENST00000338110.10:c.-30-19C>T ENSP00000336927.6:n.-30-19C>T
ENST00000395248.6:c.-30-19C>T ENSP00000378669.2:n.-30-19C>T
ENST00000566897.6:c.-49C>T ENSP00000455724.2:n.-49C>T
ENST00000568435.6:c.-30-19C>T ENSP00000457683.2:n.-30-19C>T
ENST00000338110.9:c.-959-19C>T ENSP00000336927.5:n.-959-19C>T
ENST00000395248.5:c.-887-19C>T ENSP00000378669.1:n.-887-19C>T
ENST00000562240.1:n.59-19C>T
ENST00000566280.1:n.108C>T
ENST00000566897.5:c.-834C>T ENSP00000455724.1:n.-834C>T
ENST00000568435.5:c.-815-19C>T ENSP00000457683.1:n.-815-19C>T
ENST00000575627.5:n.319C>T
ENST00000627059.2:c.-959-19C>T ENSP00000485952.1:n.-959-19C>T
NM_000034.3:c.-959-19C>T NP_000025.1:n.-959-19C>T
NM_001365304.1:c.-30-19C>T NP_001352233.1:n.-30-19C>T
NM_001365305.1:c.-49C>T NP_001352234.1:n.-49C>T
NM_001365307.1:c.-49C>T NP_001352236.1:n.-49C>T
XM_024450192.1:c.-1063-19C>T XP_024305960.1:n.-1063-19C>T
XM_024450193.1:c.-803-19C>T XP_024305961.1:n.-803-19C>T
NM_001365307.2:c.-49C>T NP_001352236.1:n.-49C>T
NM_001365304.2:c.-30-19C>T NP_001352233.1:n.-30-19C>T
NM_001365305.2:c.-49C>T NP_001352234.1:n.-49C>T