Canonical Allele Identifier: CA403672209
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7132308G>C , CM000681.2:g.7132308G>C GRCh38
NC_000019.9:g.7132319G>C , CM000681.1:g.7132319G>C GRCh37
NC_000019.8:g.7083319G>C NCBI36
NG_008852.2:g.166693C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.2692C>G MANE Select ENSP00000303830.4:p.Leu898Val
ENST00000302850.9:c.2692C>G ENSP00000303830.4:p.Leu898Val
ENST00000341500.9:c.2656C>G ENSP00000342838.4:p.Leu886Val
NM_000208.2:c.2692C>G NP_000199.2:p.Leu898Val
NM_000208.3:c.2692C>G NP_000199.2:p.Leu898Val
NM_001079817.1:c.2656C>G NP_001073285.1:p.Leu886Val
NM_001079817.2:c.2656C>G NP_001073285.1:p.Leu886Val
XM_011527988.1:c.2770C>G XP_011526290.1:p.Leu924Val
XM_011527989.1:c.2734C>G XP_011526291.1:p.Leu912Val
XM_011527988.2:c.2692C>G XP_011526290.2:p.Leu898Val
XM_011527989.3:c.2656C>G XP_011526291.2:p.Leu886Val
NM_000208.4:c.2692C>G MANE Select NP_000199.2:p.Leu898Val
NM_001079817.3:c.2656C>G NP_001073285.1:p.Leu886Val