Canonical Allele Identifier: CA16607404

Gene: ALDOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30054946G>A , CM000678.2:g.30054946G>A	GRCh38
NC_000016.9:g.30066267G>A , CM000678.1:g.30066267G>A	GRCh37
NC_000016.8:g.29973768G>A	NCBI36
NG_008010.1:g.6777G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000034.3:c.-780+19G>A	NP_000025.1:n.-780+19G>A
NM_001365304.1:c.150+19G>A	NP_001352233.1:n.150+19G>A
NM_001365304.2:c.150+19G>A	NP_001352233.1:n.150+19G>A
NM_001365305.1:c.7-226G>A	NP_001352234.1:n.7-226G>A
NM_001365305.2:c.7-226G>A	NP_001352234.1:n.7-226G>A
NM_001365307.1:c.150+19G>A	NP_001352236.1:n.150+19G>A
NM_001365307.2:c.150+19G>A	NP_001352236.1:n.150+19G>A
ENST00000338110.10:c.150+19G>A	ENSP00000336927.6:n.150+19G>A
ENST00000338110.11:c.150+19G>A	ENSP00000336927.6:n.150+19G>A
ENST00000338110.9:c.-780+19G>A	ENSP00000336927.5:n.-780+19G>A
ENST00000395248.5:c.-708+19G>A	ENSP00000378669.1:n.-708+19G>A
ENST00000395248.6:c.150+19G>A	ENSP00000378669.2:n.150+19G>A
ENST00000562240.1:n.238+19G>A
ENST00000566280.1:n.325G>A
ENST00000566897.5:c.-779-226G>A	ENSP00000455724.1:n.-779-226G>A
ENST00000566897.6:c.7-226G>A	ENSP00000455724.2:n.7-226G>A
ENST00000567249.1:n.353+19G>A
ENST00000568435.5:c.-779-226G>A	ENSP00000457683.1:n.-779-226G>A
ENST00000568435.6:c.7-226G>A	ENSP00000457683.2:n.7-226G>A
ENST00000575627.5:n.373+1447G>A
ENST00000627059.2:c.-780+19G>A	ENSP00000485952.1:n.-780+19G>A
XM_011545767.1:c.-884+19G>A	XP_011544069.1:n.-884+19G>A
XM_011545768.1:c.-624+1447G>A	XP_011544070.1:n.-624+1447G>A
XM_024450192.1:c.-884+19G>A	XP_024305960.1:n.-884+19G>A
XM_024450193.1:c.-624+19G>A	XP_024305961.1:n.-624+19G>A