Canonical Allele Identifier: CA1936327360

Gene: ADD3

Linked Data

• dbSNP Id: rs1852144895
• gnomAD v4: 10-110126282-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110126282G>T , CM000672.2:g.110126282G>T	GRCh38
NC_000010.10:g.111886040G>T , CM000672.1:g.111886040G>T	GRCh37
NC_000010.9:g.111876030G>T	NCBI36
NG_051033.1:g.134933G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356080.9:c.1522-135G>T MANE Select	ENSP00000348381.4:n.1522-135G>T
ENST00000277900.12:c.1522-135G>T	ENSP00000277900.8:n.1522-135G>T
ENST00000356080.8:c.1522-135G>T	ENSP00000348381.4:n.1522-135G>T
ENST00000360162.7:c.1522-135G>T	ENSP00000353286.3:n.1522-135G>T
ENST00000472568.5:n.559-135G>T
ENST00000479805.1:n.45-135G>T
ENST00000488799.5:n.192-135G>T
ENST00000492162.5:n.135-135G>T
ENST00000611329.1:c.1516-135G>T	ENSP00000480646.1:n.1516-135G>T
NM_001121.2:c.1522-135G>T	NP_001112.2:n.1522-135G>T
NM_016824.3:c.1522-135G>T	NP_058432.1:n.1522-135G>T
NM_019903.3:c.1522-135G>T	NP_063968.1:n.1522-135G>T
XM_005269529.1:c.1522-135G>T	XP_005269586.1:n.1522-135G>T
XM_005269530.1:c.1522-135G>T	XP_005269587.1:n.1522-135G>T
XM_005269531.3:c.1522-135G>T	XP_005269588.1:n.1522-135G>T
XM_005269533.1:c.1522-135G>T	XP_005269590.1:n.1522-135G>T
XM_005269534.3:c.1522-135G>T	XP_005269591.1:n.1522-135G>T
XM_005269535.1:c.1288-135G>T	XP_005269592.1:n.1288-135G>T
XM_006717626.1:c.1522-135G>T	XP_006717689.1:n.1522-135G>T
XM_006717627.1:c.1522-135G>T	XP_006717690.1:n.1522-135G>T
XM_006717628.2:c.1522-135G>T	XP_006717691.1:n.1522-135G>T
XM_006717629.1:c.1288-135G>T	XP_006717692.1:n.1288-135G>T
XM_011539287.1:c.1522-135G>T	XP_011537589.1:n.1522-135G>T
XM_011539288.1:c.1522-135G>T	XP_011537590.1:n.1522-135G>T
XM_011539289.1:c.796-135G>T	XP_011537591.1:n.796-135G>T
XM_011539290.1:c.796-135G>T	XP_011537592.1:n.796-135G>T
NM_001121.3:c.1522-135G>T	NP_001112.2:n.1522-135G>T
NM_001320591.1:c.1522-135G>T	NP_001307520.1:n.1522-135G>T
NM_001320592.1:c.1522-135G>T	NP_001307521.1:n.1522-135G>T
NM_001320593.1:c.1522-135G>T	NP_001307522.1:n.1522-135G>T
NM_001320594.1:c.1288-135G>T	NP_001307523.1:n.1288-135G>T
NM_016824.4:c.1522-135G>T	NP_058432.1:n.1522-135G>T
NM_019903.4:c.1522-135G>T	NP_063968.1:n.1522-135G>T
XM_024447794.1:c.1522-135G>T	XP_024303562.1:n.1522-135G>T
XM_024447795.1:c.1522-135G>T	XP_024303563.1:n.1522-135G>T
XM_024447796.1:c.1522-135G>T	XP_024303564.1:n.1522-135G>T
XM_024447797.1:c.1522-135G>T	XP_024303565.1:n.1522-135G>T
XM_024447798.1:c.1522-135G>T	XP_024303566.1:n.1522-135G>T
XM_024447799.1:c.1522-135G>T	XP_024303567.1:n.1522-135G>T
XM_024447800.1:c.1522-135G>T	XP_024303568.1:n.1522-135G>T
XM_024447801.1:c.1522-135G>T	XP_024303569.1:n.1522-135G>T
XM_024447802.1:c.1522-135G>T	XP_024303570.1:n.1522-135G>T
XM_024447803.1:c.1522-135G>T	XP_024303571.1:n.1522-135G>T
XM_024447804.1:c.1522-135G>T	XP_024303572.1:n.1522-135G>T
XM_024447805.1:c.1522-135G>T	XP_024303573.1:n.1522-135G>T
XM_024447806.1:c.1522-135G>T	XP_024303574.1:n.1522-135G>T
XM_024447807.1:c.1522-135G>T	XP_024303575.1:n.1522-135G>T
XM_024447808.1:c.1288-135G>T	XP_024303576.1:n.1288-135G>T
XM_024447809.1:c.1288-135G>T	XP_024303577.1:n.1288-135G>T
XM_024447810.1:c.1288-135G>T	XP_024303578.1:n.1288-135G>T
XM_024447811.1:c.796-135G>T	XP_024303579.1:n.796-135G>T
XM_024447812.1:c.796-135G>T	XP_024303580.1:n.796-135G>T
XM_024447813.1:c.796-135G>T	XP_024303581.1:n.796-135G>T
XM_024447814.1:c.796-135G>T	XP_024303582.1:n.796-135G>T
NM_001121.4:c.1522-135G>T	NP_001112.2:n.1522-135G>T
NM_001320591.2:c.1522-135G>T	NP_001307520.1:n.1522-135G>T
NM_001320592.2:c.1522-135G>T	NP_001307521.1:n.1522-135G>T
NM_001320593.2:c.1522-135G>T	NP_001307522.1:n.1522-135G>T
NM_001320594.2:c.1288-135G>T	NP_001307523.1:n.1288-135G>T
NM_016824.5:c.1522-135G>T MANE Select	NP_058432.1:n.1522-135G>T
NM_019903.5:c.1522-135G>T	NP_063968.1:n.1522-135G>T