Canonical Allele Identifier: CA14730145
Gene: INSR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2059807

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7166098A>G , CM000681.2:g.7166098A>G GRCh38
NC_000019.9:g.7166109A>G , CM000681.1:g.7166109A>G GRCh37
NC_000019.8:g.7117109A>G NCBI36
NG_008852.2:g.132903T>C

Transcript Alleles

HGVS Amino-acid change
NM_000208.2:c.1861+56T>C VV NP_000199.2:p.=
NM_000208.3:c.1861+56T>C VV NP_000199.2:p.=
NM_001079817.1:c.1861+56T>C VV NP_001073285.1:p.=
NM_001079817.2:c.1861+56T>C VV NP_001073285.1:p.=
XM_011527988.1:c.1939+56T>C XP_011526290.1:p.=
XM_011527989.1:c.1939+56T>C XP_011526291.1:p.=
XM_011527988.2:c.1861+56T>C XP_011526290.2:p.=
XM_011527989.3:c.1861+56T>C XP_011526291.2:p.=
NM_000208.4:c.1861+56T>C VV MANE Preferred NP_000199.2:p.=
ENST00000302850.9:c.1861+56T>C ENSP00000303830.4:p.=
ENST00000341500.9:c.1861+56T>C ENSP00000342838.4:p.=
ENST00000598216.1:n.1836+56T>C
ENST00000600492.1:n.262+56T>C ENSP00000473170.1:p.=