Canonical Allele Identifier: CA631693373
Gene: INSR HGNC NCBI

Linked Data

dbSNP Id: rs1190604917

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7182907_7182908insAA , CM000681.2:g.7182907_7182908insAA GRCh38
NC_000019.9:g.7182918_7182919insAA , CM000681.1:g.7182918_7182919insAA GRCh37
NC_000019.8:g.7133918_7133919insAA NCBI36
NG_008852.2:g.116093_116094insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.974+1408_974+1409insTT MANE Select ENSP00000303830.4:n.974+1408_974+1409insTT
ENST00000302850.9:c.974+1408_974+1409insTT ENSP00000303830.4:n.974+1408_974+1409insTT
ENST00000341500.9:c.974+1408_974+1409insTT ENSP00000342838.4:n.974+1408_974+1409insTT
ENST00000598216.1:n.949+1408_949+1409insTT
NM_000208.2:c.974+1408_974+1409insTT NP_000199.2:n.974+1408_974+1409insTT
NM_000208.3:c.974+1408_974+1409insTT NP_000199.2:n.974+1408_974+1409insTT
NM_001079817.1:c.974+1408_974+1409insTT NP_001073285.1:n.974+1408_974+1409insTT
NM_001079817.2:c.974+1408_974+1409insTT NP_001073285.1:n.974+1408_974+1409insTT
XM_011527988.1:c.1052+1408_1052+1409insTT XP_011526290.1:n.1052+1408_1052+1409insTT
XM_011527989.1:c.1052+1408_1052+1409insTT XP_011526291.1:n.1052+1408_1052+1409insTT
XM_011527988.2:c.974+1408_974+1409insTT XP_011526290.2:n.974+1408_974+1409insTT
XM_011527989.3:c.974+1408_974+1409insTT XP_011526291.2:n.974+1408_974+1409insTT
NM_000208.4:c.974+1408_974+1409insTT MANE Select NP_000199.2:n.974+1408_974+1409insTT
NM_001079817.3:c.974+1408_974+1409insTT NP_001073285.1:n.974+1408_974+1409insTT