Canonical Allele Identifier: CA365653613

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131583807A>C , CM000668.2:g.131583807A>C GRCh38
NC_000006.11:g.131904947A>C , CM000668.1:g.131904947A>C GRCh37
NC_000006.10:g.131946640A>C NCBI36
NG_007086.2:g.15583A>C
NG_031860.1:g.49417T>G
NG_031860.2:g.49417T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368087.8:c.868A>C (ARG1) MANE Select ENSP00000357066.3:p.Thr290Pro
ENST00000640973.1:c.610A>C (ARG1) ENSP00000492623.1:p.Thr204Pro
ENST00000672233.1:c.814A>C (ARG1) ENSP00000499826.1:p.Thr272Pro
ENST00000673234.1:c.*755A>C (ARG1) ENSP00000499885.1:n.*755A>C
ENST00000673427.1:c.613A>C (ARG1) ENSP00000500160.1:p.Thr205Pro
ENST00000354577.8:c.4095+3902T>G (MED23) ENSP00000346588.4:n.4095+3902T>G
ENST00000356962.2:c.892A>C (ARG1) ENSP00000349446.2:p.Thr298Pro
ENST00000368087.7:c.868A>C (ARG1) ENSP00000357066.3:p.Thr290Pro
NM_000045.3:c.868A>C (ARG1) NP_000036.2:p.Thr290Pro
NM_001244438.1:c.892A>C (ARG1) NP_001231367.1:p.Thr298Pro
NM_001270521.1:c.4077+3902T>G (MED23) NP_001257450.1:n.4077+3902T>G
NM_015979.3:c.4095+3902T>G (MED23) NP_057063.2:n.4095+3902T>G
XM_011535801.1:c.613A>C (ARG1) XP_011534103.1:p.Thr205Pro
XM_011535801.2:c.613A>C (ARG1) XP_011534103.1:p.Thr205Pro
NM_000045.4:c.868A>C (ARG1) MANE Select NP_000036.2:p.Thr290Pro
NM_001244438.2:c.892A>C (ARG1) NP_001231367.1:p.Thr298Pro
NM_001270521.2:c.4077+3902T>G (MED23) NP_001257450.1:n.4077+3902T>G
NM_001369020.1:c.613A>C (ARG1) NP_001355949.1:p.Thr205Pro
NM_015979.4:c.4095+3902T>G (MED23) NP_057063.2:n.4095+3902T>G
NR_160934.1:n.852A>C (ARG1)