Canonical Allele Identifier: CA403668751
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117307C>T , CM000681.2:g.7117307C>T GRCh38
NC_000019.9:g.7117318C>T , CM000681.1:g.7117318C>T GRCh37
NC_000019.8:g.7068318C>T NCBI36
NG_008852.2:g.181694G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3898G>A MANE Select ENSP00000303830.4:p.Glu1300Lys
ENST00000302850.9:c.3898G>A ENSP00000303830.4:p.Glu1300Lys
ENST00000341500.9:c.3862G>A ENSP00000342838.4:p.Glu1288Lys
NM_000208.2:c.3898G>A NP_000199.2:p.Glu1300Lys
NM_000208.3:c.3898G>A NP_000199.2:p.Glu1300Lys
NM_001079817.1:c.3862G>A NP_001073285.1:p.Glu1288Lys
NM_001079817.2:c.3862G>A NP_001073285.1:p.Glu1288Lys
XM_011527988.1:c.3973G>A XP_011526290.1:p.Glu1325Lys
XM_011527989.1:c.3937G>A XP_011526291.1:p.Glu1313Lys
XM_011527988.2:c.3895G>A XP_011526290.2:p.Glu1299Lys
XM_011527989.3:c.3859G>A XP_011526291.2:p.Glu1287Lys
NM_000208.4:c.3898G>A MANE Select NP_000199.2:p.Glu1300Lys
NM_001079817.3:c.3862G>A NP_001073285.1:p.Glu1288Lys