Canonical Allele Identifier: CA3636757

Gene: ADTRP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.11735664A>T , CM000668.2:g.11735664A>T	GRCh38
NC_000006.11:g.11735897A>T , CM000668.1:g.11735897A>T	GRCh37
NC_000006.10:g.11843883A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414691.8:c.410T>A MANE Select	ENSP00000404416.2:p.Ile137Asn
ENST00000229583.9:c.464T>A	ENSP00000229583.5:p.Ile155Asn
ENST00000379415.6:c.410T>A	ENSP00000368726.2:p.Ile137Asn
ENST00000414691.7:c.410T>A	ENSP00000404416.2:p.Ile137Asn
ENST00000505099.5:c.79T>A
ENST00000506810.1:c.410T>A	ENSP00000422927.1:p.Ile137Asn
ENST00000512139.5:n.273T>A
ENST00000514824.5:n.731T>A
NM_001143948.1:c.464T>A	NP_001137420.1:p.Ile155Asn
NM_032744.3:c.410T>A	NP_116133.1:p.Ile137Asn
XM_005249454.2:c.410T>A	XP_005249511.1:p.Ile137Asn
XM_011514956.1:c.410T>A	XP_011513258.1:p.Ile137Asn
XM_011514958.1:c.410T>A	XP_011513260.1:p.Ile137Asn
XM_011514959.1:c.410T>A	XP_011513261.1:p.Ile137Asn
XR_926322.1:n.723T>A
XM_005249454.3:c.410T>A	XP_005249511.1:p.Ile137Asn
XM_011514958.2:c.410T>A	XP_011513260.1:p.Ile137Asn
XM_017011377.1:c.23T>A	XP_016866866.1:p.Ile8Asn
XR_926322.2:n.723T>A
NM_001143948.2:c.464T>A	NP_001137420.1:p.Ile155Asn
NM_032744.4:c.410T>A MANE Select	NP_116133.1:p.Ile137Asn