Canonical Allele Identifier: CA1580440279
Gene: ALDH7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126544702_126544703delinsTA , CM000667.2:g.126544702_126544703delinsTA GRCh38
NC_000005.9:g.125880394_125880395delinsTA , CM000667.1:g.125880394_125880395delinsTA GRCh37
NC_000005.8:g.125908293_125908294delinsTA NCBI36
NG_008600.2:g.55688_55689delinsTA
NG_008600.3:g.55688_55689delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000409134.8:c.*262_*263delinsTA MANE Select ENSP00000387123.3:n.*262_*263delinsTA
ENST00000635851.1:c.1563+1621_1563+1622delinsTA
ENST00000636743.1:c.*262_*263delinsTA ENSP00000489725.1:n.*262_*263delinsTA
ENST00000636808.1:c.*1691_*1692delinsTA ENSP00000490833.1:n.*1691_*1692delinsTA
ENST00000636872.1:c.2042_2043delinsTA ENSP00000490919.1:n.2042_2043delinsTA
ENST00000636879.1:c.*262_*263delinsTA ENSP00000490811.1:n.*262_*263delinsTA
ENST00000636886.1:c.*262_*263delinsTA ENSP00000490371.1:n.*262_*263delinsTA
ENST00000637206.1:c.*262_*263delinsTA ENSP00000489895.1:n.*262_*263delinsTA
ENST00000637272.1:c.*262_*263delinsTA ENSP00000489686.1:n.*262_*263delinsTA
ENST00000637782.1:c.1565+1621_1565+1622delinsTA ENSP00000490024.1:n.1565+1621_1565+1622delinsTA
ENST00000409134.7:c.*262_*263delinsTA ENSP00000387123.3:n.*262_*263delinsTA
ENST00000447989.6:c.*262_*263delinsTA ENSP00000414132.2:n.*262_*263delinsTA
ENST00000553117.5:c.*262_*263delinsTA ENSP00000448593.1:n.*262_*263delinsTA
NM_001182.4:c.*262_*263delinsTA NP_001173.2:n.*262_*263delinsTA
NM_001201377.1:c.*262_*263delinsTA NP_001188306.1:n.*262_*263delinsTA
NM_001202404.1:c.*262_*263delinsTA NP_001189333.1:n.*262_*263delinsTA
XM_011543417.2:c.*262_*263delinsTA XP_011541719.1:n.*262_*263delinsTA
NM_001182.5:c.*262_*263delinsTA MANE Select NP_001173.2:n.*262_*263delinsTA
NM_001201377.2:c.*262_*263delinsTA NP_001188306.1:n.*262_*263delinsTA
NM_001202404.2:c.*262_*263delinsTA NP_001189333.2:n.*262_*263delinsTA