Canonical Allele Identifier: CA403668218
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117069G>A , CM000681.2:g.7117069G>A GRCh38
NC_000019.9:g.7117080G>A , CM000681.1:g.7117080G>A GRCh37
NC_000019.8:g.7068080G>A NCBI36
NG_008852.2:g.181932C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.4136C>T MANE Select ENSP00000303830.4:p.Ser1379Phe
ENST00000302850.9:c.4136C>T ENSP00000303830.4:p.Ser1379Phe
ENST00000341500.9:c.4100C>T ENSP00000342838.4:p.Ser1367Phe
NM_000208.2:c.4136C>T NP_000199.2:p.Ser1379Phe
NM_000208.3:c.4136C>T NP_000199.2:p.Ser1379Phe
NM_001079817.1:c.4100C>T NP_001073285.1:p.Ser1367Phe
NM_001079817.2:c.4100C>T NP_001073285.1:p.Ser1367Phe
XM_011527988.1:c.4211C>T XP_011526290.1:p.Ser1404Phe
XM_011527989.1:c.4175C>T XP_011526291.1:p.Ser1392Phe
XM_011527988.2:c.4133C>T XP_011526290.2:p.Ser1378Phe
XM_011527989.3:c.4097C>T XP_011526291.2:p.Ser1366Phe
NM_000208.4:c.4136C>T MANE Select NP_000199.2:p.Ser1379Phe
NM_001079817.3:c.4100C>T NP_001073285.1:p.Ser1367Phe