Canonical Allele Identifier: CA403671473
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7125519A>C , CM000681.2:g.7125519A>C GRCh38
NC_000019.9:g.7125530A>C , CM000681.1:g.7125530A>C GRCh37
NC_000019.8:g.7076530A>C NCBI36
NG_008852.2:g.173482T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3022T>G MANE Select ENSP00000303830.4:p.Cys1008Gly
ENST00000302850.9:c.3022T>G ENSP00000303830.4:p.Cys1008Gly
ENST00000341500.9:c.2986T>G ENSP00000342838.4:p.Cys996Gly
NM_000208.2:c.3022T>G NP_000199.2:p.Cys1008Gly
NM_000208.3:c.3022T>G NP_000199.2:p.Cys1008Gly
NM_001079817.1:c.2986T>G NP_001073285.1:p.Cys996Gly
NM_001079817.2:c.2986T>G NP_001073285.1:p.Cys996Gly
XM_011527988.1:c.3097T>G XP_011526290.1:p.Cys1033Gly
XM_011527989.1:c.3061T>G XP_011526291.1:p.Cys1021Gly
XM_011527988.2:c.3019T>G XP_011526290.2:p.Cys1007Gly
XM_011527989.3:c.2983T>G XP_011526291.2:p.Cys995Gly
NM_000208.4:c.3022T>G MANE Select NP_000199.2:p.Cys1008Gly
NM_001079817.3:c.2986T>G NP_001073285.1:p.Cys996Gly