Canonical Allele Identifier: CA2578741093

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131583743del , CM000668.2:g.131583743del GRCh38
NC_000006.11:g.131904883del , CM000668.1:g.131904883del GRCh37
NC_000006.10:g.131946576del NCBI36
NG_007086.2:g.15519del
NG_031860.1:g.49483del
NG_031860.2:g.49483del

Transcript Alleles

HGVS Amino-acid change
ENST00000368087.8:c.804del (ARG1)
ENST00000640973.1:c.605-59del (ARG1) ENSP00000492623.1:n.605-59del
ENST00000672233.1:c.750del (ARG1)
ENST00000673234.1:c.*691del (ARG1)
ENST00000673427.1:c.549del (ARG1)
ENST00000354577.8:c.4095+3968del (MED23) ENSP00000346588.4:n.4095+3968del
ENST00000356962.2:c.828del (ARG1)
ENST00000368087.7:c.804del (ARG1)
NM_000045.3:c.804del (ARG1)
NM_001244438.1:c.828del (ARG1)
NM_001270521.1:c.4077+3968del (MED23) NP_001257450.1:n.4077+3968del
NM_015979.3:c.4095+3968del (MED23) NP_057063.2:n.4095+3968del
XM_011535801.1:c.549del (ARG1)
XM_011535801.2:c.549del (ARG1)
NM_000045.4:c.804del (ARG1)
NM_001244438.2:c.828del (ARG1)
NM_001270521.2:c.4077+3968del (MED23) NP_001257450.1:n.4077+3968del
NM_001369020.1:c.549del (ARG1)
NM_015979.4:c.4095+3968del (MED23) NP_057063.2:n.4095+3968del
NR_160934.1:n.788del (ARG1)