Canonical Allele Identifier: CA2739270476
Community Standard Title: NM_015459.5(ATL3):c.1139_1140del (p.Pro380ArgfsTer9)
Gene: ATL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.63631439_63631440del , CM000673.2:g.63631439_63631440del GRCh38
NC_000011.9:g.63398911_63398912del , CM000673.1:g.63398911_63398912del GRCh37
NC_000011.8:g.63155487_63155488del NCBI36
NG_033985.1:g.45535_45536del

Transcript Alleles

HGVS Amino-acid Change
NM_015459.5:c.1139_1140del MANE Select NP_056274.3:p.Pro380ArgfsTer9
ENST00000398868.8:c.1139_1140del MANE Select ENSP00000381844.3:p.Pro380ArgfsTer9
NM_001290048.1:c.1085_1086del NP_001276977.1:p.Pro362ArgfsTer9
NM_001290048.2:c.1085_1086del NP_001276977.1:p.Pro362ArgfsTer9
NM_015459.4:c.1139_1140del NP_056274.3:p.Pro380ArgfsTer9
ENST00000398868.7:c.1139_1140del ENSP00000381844.3:p.Pro380ArgfsTer9
ENST00000538786.1:c.1085_1086del ENSP00000437593.1:p.Pro362ArgfsTer9
XM_006718493.1:c.1082_1083del XP_006718556.1:p.Pro361ArgfsTer9
XM_011544902.1:c.551_552del XP_011543204.1:p.Pro184ArgfsTer9
XM_024448428.1:c.551_552del XP_024304196.1:p.Pro184ArgfsTer9
XR_001748255.1:n.325-6052_325-6051del