Canonical Allele Identifier: CA304866078
Gene: INSR HGNC NCBI

Linked Data

dbSNP Id: rs765415858
gnomAD v4: 19-7116954-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7116954G>A , CM000681.2:g.7116954G>A GRCh38
NC_000019.9:g.7116965G>A , CM000681.1:g.7116965G>A GRCh37
NC_000019.8:g.7067965G>A NCBI36
NG_008852.2:g.182047C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.*102C>T MANE Select ENSP00000303830.4:n.*102C>T
ENST00000302850.9:c.*102C>T ENSP00000303830.4:n.*102C>T
ENST00000341500.9:c.*102C>T ENSP00000342838.4:n.*102C>T
NM_000208.2:c.*102C>T NP_000199.2:n.*102C>T
NM_000208.3:c.*102C>T NP_000199.2:n.*102C>T
NM_001079817.1:c.*102C>T NP_001073285.1:n.*102C>T
NM_001079817.2:c.*102C>T NP_001073285.1:n.*102C>T
XM_011527988.1:c.*102C>T XP_011526290.1:n.*102C>T
XM_011527989.1:c.*102C>T XP_011526291.1:n.*102C>T
XM_011527988.2:c.*102C>T XP_011526290.2:n.*102C>T
XM_011527989.3:c.*102C>T XP_011526291.2:n.*102C>T
NM_000208.4:c.*102C>T MANE Select NP_000199.2:n.*102C>T
NM_001079817.3:c.*102C>T NP_001073285.1:n.*102C>T