Canonical Allele Identifier: CA2587920792
Gene: INSR HGNC NCBI

Linked Data

gnomAD v4: 19-7116819-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7116819A>T , CM000681.2:g.7116819A>T GRCh38
NC_000019.9:g.7116830A>T , CM000681.1:g.7116830A>T GRCh37
NC_000019.8:g.7067830A>T NCBI36
NG_008852.2:g.182182T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.*237T>A MANE Select ENSP00000303830.4:n.*237T>A
ENST00000302850.9:c.*237T>A ENSP00000303830.4:n.*237T>A
ENST00000341500.9:c.*237T>A ENSP00000342838.4:n.*237T>A
NM_000208.2:c.*237T>A NP_000199.2:n.*237T>A
NM_000208.3:c.*237T>A NP_000199.2:n.*237T>A
NM_001079817.1:c.*237T>A NP_001073285.1:n.*237T>A
NM_001079817.2:c.*237T>A NP_001073285.1:n.*237T>A
XM_011527988.1:c.*237T>A XP_011526290.1:n.*237T>A
XM_011527989.1:c.*237T>A XP_011526291.1:n.*237T>A
XM_011527988.2:c.*237T>A XP_011526290.2:n.*237T>A
XM_011527989.3:c.*237T>A XP_011526291.2:n.*237T>A
NM_000208.4:c.*237T>A MANE Select NP_000199.2:n.*237T>A
NM_001079817.3:c.*237T>A NP_001073285.1:n.*237T>A
Search 100 bp 5'
Search 100 bp 3'