Canonical Allele Identifier: CA2320767930
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7125349A= , CM000681.2:g.7125349A= GRCh38
NC_000019.9:g.7125360A= , CM000681.1:g.7125360A= GRCh37
NC_000019.8:g.7076360A= NCBI36
NG_008852.2:g.173652T=

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.3192T= MANE Select ENSP00000303830.4:p.Ser1064=
ENST00000302850.9:c.3192T= ENSP00000303830.4:p.Ser1064=
ENST00000341500.9:c.3156T= ENSP00000342838.4:p.Ser1052=
ENST00000593970.1:n.38T=
NM_000208.2:c.3192T= NP_000199.2:p.Ser1064=
NM_000208.3:c.3192T= NP_000199.2:p.Ser1064=
NM_001079817.1:c.3156T= NP_001073285.1:p.Ser1052=
NM_001079817.2:c.3156T= NP_001073285.1:p.Ser1052=
XM_011527988.1:c.3267T= XP_011526290.1:p.Ser1089=
XM_011527989.1:c.3231T= XP_011526291.1:p.Ser1077=
XM_011527988.2:c.3189T= XP_011526290.2:p.Ser1063=
XM_011527989.3:c.3153T= XP_011526291.2:p.Ser1051=
NM_000208.4:c.3192T= MANE Select NP_000199.2:p.Ser1064=
NM_001079817.3:c.3156T= NP_001073285.1:p.Ser1052=