Canonical Allele Identifier: CA884174936
Gene: INSR HGNC NCBI

Linked Data

dbSNP Id: rs1269943104

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7116903_7116911dup , CM000681.2:g.7116903_7116911dup GRCh38
NC_000019.9:g.7116914_7116922dup , CM000681.1:g.7116914_7116922dup GRCh37
NC_000019.8:g.7067914_7067922dup NCBI36
NG_008852.2:g.182090_182098dup

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.*145_*153dup MANE Select ENSP00000303830.4:n.*145_*153dup
ENST00000302850.9:c.*145_*153dup ENSP00000303830.4:n.*145_*153dup
ENST00000341500.9:c.*145_*153dup ENSP00000342838.4:n.*145_*153dup
NM_000208.2:c.*145_*153dup NP_000199.2:n.*145_*153dup
NM_000208.3:c.*145_*153dup NP_000199.2:n.*145_*153dup
NM_001079817.1:c.*145_*153dup NP_001073285.1:n.*145_*153dup
NM_001079817.2:c.*145_*153dup NP_001073285.1:n.*145_*153dup
XM_011527988.1:c.*145_*153dup XP_011526290.1:n.*145_*153dup
XM_011527989.1:c.*145_*153dup XP_011526291.1:n.*145_*153dup
XM_011527988.2:c.*145_*153dup XP_011526290.2:n.*145_*153dup
XM_011527989.3:c.*145_*153dup XP_011526291.2:n.*145_*153dup
NM_000208.4:c.*145_*153dup MANE Select NP_000199.2:n.*145_*153dup
NM_001079817.3:c.*145_*153dup NP_001073285.1:n.*145_*153dup