Canonical Allele Identifier: CA14633734
Gene: INSR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2252673

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7150407C>G , CM000681.2:g.7150407C>G GRCh38
NC_000019.8:g.7101418C>G NCBI36
NC_000019.9:g.7150418C>G , CM000681.1:g.7150418C>G GRCh37
NG_008852.2:g.148594G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.9:c.2267+90G>C ENSP00000303830.4:p.=
ENST00000341500.9:c.2231+2319G>C ENSP00000342838.4:p.=
NM_000208.2:c.2267+90G>C
NM_000208.3:c.2267+90G>C NP_000199.2:p.=
NM_001079817.1:c.2231+2319G>C
NM_001079817.2:c.2231+2319G>C NP_001073285.1:p.=
XM_011527988.1:c.2345+90G>C XP_011526290.1:p.=
XM_011527989.1:c.2309+2319G>C XP_011526291.1:p.=