Canonical Allele Identifier: CA2513715617

Gene: AADAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.170073928A>G , CM000666.2:g.170073928A>G	GRCh38
NC_000004.11:g.170995079A>G , CM000666.1:g.170995079A>G	GRCh37
NC_000004.10:g.171231654A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337664.9:c.445-583T>C MANE Select	ENSP00000336808.4:n.445-583T>C
ENST00000337664.8:c.445-583T>C	ENSP00000336808.4:n.445-583T>C
ENST00000353187.6:c.445-583T>C	ENSP00000226840.4:n.445-583T>C
ENST00000502392.1:c.445-583T>C	ENSP00000423843.1:n.445-583T>C
ENST00000505906.1:n.244-583T>C
ENST00000507375.5:c.445-583T>C	ENSP00000421389.1:n.445-583T>C
ENST00000509167.5:c.457-583T>C	ENSP00000423190.1:n.457-583T>C
ENST00000510340.5:c.418-583T>C	ENSP00000425067.1:n.418-583T>C
ENST00000515480.5:c.445-583T>C	ENSP00000423341.1:n.445-583T>C
NM_001286682.1:c.457-583T>C	NP_001273611.1:n.457-583T>C
NM_001286683.1:c.445-583T>C	NP_001273612.1:n.445-583T>C
NM_016228.3:c.445-583T>C	NP_057312.1:n.445-583T>C
NM_182662.1:c.445-583T>C	NP_872603.1:n.445-583T>C
XM_006714231.2:c.562-583T>C	XP_006714294.1:n.562-583T>C
XM_011532020.1:c.100-583T>C	XP_011530322.1:n.100-583T>C
XM_011532020.2:c.100-583T>C	XP_011530322.1:n.100-583T>C
XM_024454077.1:c.445-583T>C	XP_024309845.1:n.445-583T>C
NM_016228.4:c.445-583T>C MANE Select	NP_057312.1:n.445-583T>C
NM_001286682.2:c.457-583T>C	NP_001273611.1:n.457-583T>C
NM_182662.2:c.445-583T>C	NP_872603.1:n.445-583T>C