Canonical Allele Identifier: CA2320776199
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7142973G= , CM000681.2:g.7142973G= GRCh38
NC_000019.9:g.7142984G= , CM000681.1:g.7142984G= GRCh37
NC_000019.8:g.7093984G= NCBI36
NG_008852.2:g.156028C=

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.2385C= MANE Select ENSP00000303830.4:p.His795=
ENST00000302850.9:c.2385C= ENSP00000303830.4:p.His795=
ENST00000341500.9:c.2349C= ENSP00000342838.4:p.His783=
ENST00000597211.1:n.68C=
NM_000208.2:c.2385C= NP_000199.2:p.His795=
NM_000208.3:c.2385C= NP_000199.2:p.His795=
NM_001079817.1:c.2349C= NP_001073285.1:p.His783=
NM_001079817.2:c.2349C= NP_001073285.1:p.His783=
XM_011527988.1:c.2463C= XP_011526290.1:p.His821=
XM_011527989.1:c.2427C= XP_011526291.1:p.His809=
XM_011527988.2:c.2385C= XP_011526290.2:p.His795=
XM_011527989.3:c.2349C= XP_011526291.2:p.His783=
NM_000208.4:c.2385C= MANE Select NP_000199.2:p.His795=
NM_001079817.3:c.2349C= NP_001073285.1:p.His783=