Canonical Allele Identifier: CA365653625

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131583814C>T , CM000668.2:g.131583814C>T GRCh38
NC_000006.11:g.131904954C>T , CM000668.1:g.131904954C>T GRCh37
NC_000006.10:g.131946647C>T NCBI36
NG_007086.2:g.15590C>T
NG_031860.1:g.49410G>A
NG_031860.2:g.49410G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368087.8:c.875C>T (ARG1) MANE Select ENSP00000357066.3:p.Thr292Ile
ENST00000640973.1:c.617C>T (ARG1) ENSP00000492623.1:p.Thr206Ile
ENST00000672233.1:c.821C>T (ARG1) ENSP00000499826.1:p.Thr274Ile
ENST00000673234.1:c.*762C>T (ARG1) ENSP00000499885.1:n.*762C>T
ENST00000673427.1:c.620C>T (ARG1) ENSP00000500160.1:p.Thr207Ile
ENST00000354577.8:c.4095+3895G>A (MED23) ENSP00000346588.4:n.4095+3895G>A
ENST00000356962.2:c.899C>T (ARG1) ENSP00000349446.2:p.Thr300Ile
ENST00000368087.7:c.875C>T (ARG1) ENSP00000357066.3:p.Thr292Ile
NM_000045.3:c.875C>T (ARG1) NP_000036.2:p.Thr292Ile
NM_001244438.1:c.899C>T (ARG1) NP_001231367.1:p.Thr300Ile
NM_001270521.1:c.4077+3895G>A (MED23) NP_001257450.1:n.4077+3895G>A
NM_015979.3:c.4095+3895G>A (MED23) NP_057063.2:n.4095+3895G>A
XM_011535801.1:c.620C>T (ARG1) XP_011534103.1:p.Thr207Ile
XM_011535801.2:c.620C>T (ARG1) XP_011534103.1:p.Thr207Ile
NM_000045.4:c.875C>T (ARG1) MANE Select NP_000036.2:p.Thr292Ile
NM_001244438.2:c.899C>T (ARG1) NP_001231367.1:p.Thr300Ile
NM_001270521.2:c.4077+3895G>A (MED23) NP_001257450.1:n.4077+3895G>A
NM_001369020.1:c.620C>T (ARG1) NP_001355949.1:p.Thr207Ile
NM_015979.4:c.4095+3895G>A (MED23) NP_057063.2:n.4095+3895G>A
NR_160934.1:n.859C>T (ARG1)