Canonical Allele Identifier: CA403672176
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7132292T>G , CM000681.2:g.7132292T>G GRCh38
NC_000019.9:g.7132303T>G , CM000681.1:g.7132303T>G GRCh37
NC_000019.8:g.7083303T>G NCBI36
NG_008852.2:g.166709A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.2708A>C MANE Select ENSP00000303830.4:p.Lys903Thr
ENST00000302850.9:c.2708A>C ENSP00000303830.4:p.Lys903Thr
ENST00000341500.9:c.2672A>C ENSP00000342838.4:p.Lys891Thr
NM_000208.2:c.2708A>C NP_000199.2:p.Lys903Thr
NM_000208.3:c.2708A>C NP_000199.2:p.Lys903Thr
NM_001079817.1:c.2672A>C NP_001073285.1:p.Lys891Thr
NM_001079817.2:c.2672A>C NP_001073285.1:p.Lys891Thr
XM_011527988.1:c.2786A>C XP_011526290.1:p.Lys929Thr
XM_011527989.1:c.2750A>C XP_011526291.1:p.Lys917Thr
XM_011527988.2:c.2708A>C XP_011526290.2:p.Lys903Thr
XM_011527989.3:c.2672A>C XP_011526291.2:p.Lys891Thr
NM_000208.4:c.2708A>C MANE Select NP_000199.2:p.Lys903Thr
NM_001079817.3:c.2672A>C NP_001073285.1:p.Lys891Thr