Canonical Allele Identifier: CA3999388

Linked Data

dbSNP Id: rs773398169

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131583774A>C , CM000668.2:g.131583774A>C GRCh38
NC_000006.11:g.131904914A>C , CM000668.1:g.131904914A>C GRCh37
NC_000006.10:g.131946607A>C NCBI36
NG_007086.2:g.15550A>C
NG_031860.1:g.49450T>G
NG_031860.2:g.49450T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368087.8:c.835A>C (ARG1) MANE Select ENSP00000357066.3:p.Asn279His
ENST00000640973.1:c.605-28A>C (ARG1) ENSP00000492623.1:n.605-28A>C
ENST00000672233.1:c.781A>C (ARG1) ENSP00000499826.1:p.Asn261His
ENST00000673234.1:c.*722A>C (ARG1) ENSP00000499885.1:n.*722A>C
ENST00000673427.1:c.580A>C (ARG1) ENSP00000500160.1:p.Asn194His
ENST00000354577.8:c.4095+3935T>G (MED23) ENSP00000346588.4:n.4095+3935T>G
ENST00000356962.2:c.859A>C (ARG1) ENSP00000349446.2:p.Asn287His
ENST00000368087.7:c.835A>C (ARG1) ENSP00000357066.3:p.Asn279His
NM_000045.3:c.835A>C (ARG1) NP_000036.2:p.Asn279His
NM_001244438.1:c.859A>C (ARG1) NP_001231367.1:p.Asn287His
NM_001270521.1:c.4077+3935T>G (MED23) NP_001257450.1:n.4077+3935T>G
NM_015979.3:c.4095+3935T>G (MED23) NP_057063.2:n.4095+3935T>G
XM_011535801.1:c.580A>C (ARG1) XP_011534103.1:p.Asn194His
XM_011535801.2:c.580A>C (ARG1) XP_011534103.1:p.Asn194His
NM_000045.4:c.835A>C (ARG1) MANE Select NP_000036.2:p.Asn279His
NM_001244438.2:c.859A>C (ARG1) NP_001231367.1:p.Asn287His
NM_001270521.2:c.4077+3935T>G (MED23) NP_001257450.1:n.4077+3935T>G
NM_001369020.1:c.580A>C (ARG1) NP_001355949.1:p.Asn194His
NM_015979.4:c.4095+3935T>G (MED23) NP_057063.2:n.4095+3935T>G
NR_160934.1:n.819A>C (ARG1)