Canonical Allele Identifier: CA1512245411

Gene: AADAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.170073912A= , CM000666.2:g.170073912A=	GRCh38
NC_000004.11:g.170995063A= , CM000666.1:g.170995063A=	GRCh37
NC_000004.10:g.171231638A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337664.9:c.445-567T= MANE Select	ENSP00000336808.4:n.445-567T=
ENST00000337664.8:c.445-567T=	ENSP00000336808.4:n.445-567T=
ENST00000353187.6:c.445-567T=	ENSP00000226840.4:n.445-567T=
ENST00000502392.1:c.445-567T=	ENSP00000423843.1:n.445-567T=
ENST00000505906.1:n.244-567T=
ENST00000507375.5:c.445-567T=	ENSP00000421389.1:n.445-567T=
ENST00000509167.5:c.457-567T=	ENSP00000423190.1:n.457-567T=
ENST00000510340.5:c.418-567T=	ENSP00000425067.1:n.418-567T=
ENST00000515480.5:c.445-567T=	ENSP00000423341.1:n.445-567T=
NM_001286682.1:c.457-567T=	NP_001273611.1:n.457-567T=
NM_001286683.1:c.445-567T=	NP_001273612.1:n.445-567T=
NM_016228.3:c.445-567T=	NP_057312.1:n.445-567T=
NM_182662.1:c.445-567T=	NP_872603.1:n.445-567T=
XM_006714231.2:c.562-567T=	XP_006714294.1:n.562-567T=
XM_011532020.1:c.100-567T=	XP_011530322.1:n.100-567T=
XM_011532020.2:c.100-567T=	XP_011530322.1:n.100-567T=
XM_024454077.1:c.445-567T=	XP_024309845.1:n.445-567T=
NM_016228.4:c.445-567T= MANE Select	NP_057312.1:n.445-567T=
NM_001286682.2:c.457-567T=	NP_001273611.1:n.457-567T=
NM_182662.2:c.445-567T=	NP_872603.1:n.445-567T=