Canonical Allele Identifier: CA2813449671
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7116781_7116807dup , CM000681.2:g.7116781_7116807dup GRCh38
NC_000019.9:g.7116792_7116818dup , CM000681.1:g.7116792_7116818dup GRCh37
NC_000019.8:g.7067792_7067818dup NCBI36
NG_008852.2:g.182194_182220dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.*249_*275dup MANE Select ENSP00000303830.4:n.*249_*275dup
ENST00000302850.9:c.*249_*275dup ENSP00000303830.4:n.*249_*275dup
ENST00000341500.9:c.*249_*275dup ENSP00000342838.4:n.*249_*275dup
NM_000208.2:c.*249_*275dup NP_000199.2:n.*249_*275dup
NM_000208.3:c.*249_*275dup NP_000199.2:n.*249_*275dup
NM_001079817.1:c.*249_*275dup NP_001073285.1:n.*249_*275dup
NM_001079817.2:c.*249_*275dup NP_001073285.1:n.*249_*275dup
XM_011527988.1:c.*249_*275dup XP_011526290.1:n.*249_*275dup
XM_011527989.1:c.*249_*275dup XP_011526291.1:n.*249_*275dup
XM_011527988.2:c.*249_*275dup XP_011526290.2:n.*249_*275dup
XM_011527989.3:c.*249_*275dup XP_011526291.2:n.*249_*275dup
NM_000208.4:c.*249_*275dup MANE Select NP_000199.2:n.*249_*275dup
NM_001079817.3:c.*249_*275dup NP_001073285.1:n.*249_*275dup