Canonical Allele Identifier: CA631723754
Gene: INSR HGNC NCBI

Linked Data

dbSNP Id: rs1262943746

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7170763dup , CM000681.2:g.7170763dup GRCh38
NC_000019.9:g.7170774dup , CM000681.1:g.7170774dup GRCh37
NC_000019.8:g.7121774dup NCBI36
NG_008852.2:g.128243dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.1269-7dup MANE Select ENSP00000303830.4:n.1269-7dup
ENST00000302850.9:c.1269-7dup ENSP00000303830.4:n.1269-7dup
ENST00000341500.9:c.1269-7dup ENSP00000342838.4:n.1269-7dup
ENST00000598216.1:n.1244-7dup
NM_000208.2:c.1269-7dup NP_000199.2:n.1269-7dup
NM_000208.3:c.1269-7dup NP_000199.2:n.1269-7dup
NM_001079817.1:c.1269-7dup NP_001073285.1:n.1269-7dup
NM_001079817.2:c.1269-7dup NP_001073285.1:n.1269-7dup
XM_011527988.1:c.1347-7dup XP_011526290.1:n.1347-7dup
XM_011527989.1:c.1347-7dup XP_011526291.1:n.1347-7dup
XM_011527988.2:c.1269-7dup XP_011526290.2:n.1269-7dup
XM_011527989.3:c.1269-7dup XP_011526291.2:n.1269-7dup
NM_000208.4:c.1269-7dup MANE Select NP_000199.2:n.1269-7dup
NM_001079817.3:c.1269-7dup NP_001073285.1:n.1269-7dup