Canonical Allele Identifier: CA403671966
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7132190G>C , CM000681.2:g.7132190G>C GRCh38
NC_000019.9:g.7132201G>C , CM000681.1:g.7132201G>C GRCh37
NC_000019.8:g.7083201G>C NCBI36
NG_008852.2:g.166811C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.2810C>G MANE Select ENSP00000303830.4:p.Thr937Arg
ENST00000302850.9:c.2810C>G ENSP00000303830.4:p.Thr937Arg
ENST00000341500.9:c.2774C>G ENSP00000342838.4:p.Thr925Arg
NM_000208.2:c.2810C>G NP_000199.2:p.Thr937Arg
NM_000208.3:c.2810C>G NP_000199.2:p.Thr937Arg
NM_001079817.1:c.2774C>G NP_001073285.1:p.Thr925Arg
NM_001079817.2:c.2774C>G NP_001073285.1:p.Thr925Arg
XM_011527988.1:c.2888C>G XP_011526290.1:p.Thr963Arg
XM_011527989.1:c.2852C>G XP_011526291.1:p.Thr951Arg
XM_011527988.2:c.2810C>G XP_011526290.2:p.Thr937Arg
XM_011527989.3:c.2774C>G XP_011526291.2:p.Thr925Arg
NM_000208.4:c.2810C>G MANE Select NP_000199.2:p.Thr937Arg
NM_001079817.3:c.2774C>G NP_001073285.1:p.Thr925Arg