Canonical Allele Identifier: CA403668265
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117094C>G , CM000681.2:g.7117094C>G GRCh38
NC_000019.9:g.7117105C>G , CM000681.1:g.7117105C>G GRCh37
NC_000019.8:g.7068105C>G NCBI36
NG_008852.2:g.181907G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.4111G>C MANE Select ENSP00000303830.4:p.Gly1371Arg
ENST00000302850.9:c.4111G>C ENSP00000303830.4:p.Gly1371Arg
ENST00000341500.9:c.4075G>C ENSP00000342838.4:p.Gly1359Arg
NM_000208.2:c.4111G>C NP_000199.2:p.Gly1371Arg
NM_000208.3:c.4111G>C NP_000199.2:p.Gly1371Arg
NM_001079817.1:c.4075G>C NP_001073285.1:p.Gly1359Arg
NM_001079817.2:c.4075G>C NP_001073285.1:p.Gly1359Arg
XM_011527988.1:c.4186G>C XP_011526290.1:p.Gly1396Arg
XM_011527989.1:c.4150G>C XP_011526291.1:p.Gly1384Arg
XM_011527988.2:c.4108G>C XP_011526290.2:p.Gly1370Arg
XM_011527989.3:c.4072G>C XP_011526291.2:p.Gly1358Arg
NM_000208.4:c.4111G>C MANE Select NP_000199.2:p.Gly1371Arg
NM_001079817.3:c.4075G>C NP_001073285.1:p.Gly1359Arg