Canonical Allele Identifier: CA2680353527

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131583545_131583546dup , CM000668.2:g.131583545_131583546dup GRCh38
NC_000006.11:g.131904685_131904686dup , CM000668.1:g.131904685_131904686dup GRCh37
NC_000006.10:g.131946378_131946379dup NCBI36
NG_007086.2:g.15321_15322dup
NG_031860.1:g.49684_49685dup
NG_031860.2:g.49684_49685dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368087.8:c.802+54_802+55dup (ARG1) MANE Select ENSP00000357066.3:n.802+54_802+55dup
ENST00000640973.1:c.605-257_605-256dup (ARG1) ENSP00000492623.1:n.605-257_605-256dup
ENST00000672233.1:c.748+54_748+55dup (ARG1) ENSP00000499826.1:n.748+54_748+55dup
ENST00000673234.1:c.*689+54_*689+55dup (ARG1) ENSP00000499885.1:n.*689+54_*689+55dup
ENST00000673427.1:c.547+54_547+55dup (ARG1) ENSP00000500160.1:n.547+54_547+55dup
ENST00000354577.8:c.4095+4169_4095+4170dup (MED23) ENSP00000346588.4:n.4095+4169_4095+4170dup
ENST00000356962.2:c.826+54_826+55dup (ARG1) ENSP00000349446.2:n.826+54_826+55dup
ENST00000368087.7:c.802+54_802+55dup (ARG1) ENSP00000357066.3:n.802+54_802+55dup
NM_000045.3:c.802+54_802+55dup (ARG1) NP_000036.2:n.802+54_802+55dup
NM_001244438.1:c.826+54_826+55dup (ARG1) NP_001231367.1:n.826+54_826+55dup
NM_001270521.1:c.4077+4169_4077+4170dup (MED23) NP_001257450.1:n.4077+4169_4077+4170dup
NM_015979.3:c.4095+4169_4095+4170dup (MED23) NP_057063.2:n.4095+4169_4095+4170dup
XM_011535801.1:c.547+54_547+55dup (ARG1) XP_011534103.1:n.547+54_547+55dup
XM_011535801.2:c.547+54_547+55dup (ARG1) XP_011534103.1:n.547+54_547+55dup
NM_000045.4:c.802+54_802+55dup (ARG1) MANE Select NP_000036.2:n.802+54_802+55dup
NM_001244438.2:c.826+54_826+55dup (ARG1) NP_001231367.1:n.826+54_826+55dup
NM_001270521.2:c.4077+4169_4077+4170dup (MED23) NP_001257450.1:n.4077+4169_4077+4170dup
NM_001369020.1:c.547+54_547+55dup (ARG1) NP_001355949.1:n.547+54_547+55dup
NM_015979.4:c.4095+4169_4095+4170dup (MED23) NP_057063.2:n.4095+4169_4095+4170dup
NR_160934.1:n.786+54_786+55dup (ARG1)