Canonical Allele Identifier: CA993111890

Gene: INSR

Linked Data

• gnomAD v3: 19-7166030-T-C
• gnomAD v4: 19-7166030-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166030T>C , CM000681.2:g.7166030T>C	GRCh38
NC_000019.9:g.7166041T>C , CM000681.1:g.7166041T>C	GRCh37
NC_000019.8:g.7117041T>C	NCBI36
NG_008852.2:g.132971A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1861+124A>G MANE Select	ENSP00000303830.4:n.1861+124A>G
ENST00000302850.9:c.1861+124A>G	ENSP00000303830.4:n.1861+124A>G
ENST00000341500.9:c.1861+124A>G	ENSP00000342838.4:n.1861+124A>G
ENST00000598216.1:n.1836+124A>G
ENST00000600492.1:c.262+124A>G	ENSP00000473170.1:n.262+124A>G
NM_000208.2:c.1861+124A>G	NP_000199.2:n.1861+124A>G
NM_000208.3:c.1861+124A>G	NP_000199.2:n.1861+124A>G
NM_001079817.1:c.1861+124A>G	NP_001073285.1:n.1861+124A>G
NM_001079817.2:c.1861+124A>G	NP_001073285.1:n.1861+124A>G
XM_011527988.1:c.1939+124A>G	XP_011526290.1:n.1939+124A>G
XM_011527989.1:c.1939+124A>G	XP_011526291.1:n.1939+124A>G
XM_011527988.2:c.1861+124A>G	XP_011526290.2:n.1861+124A>G
XM_011527989.3:c.1861+124A>G	XP_011526291.2:n.1861+124A>G
NM_000208.4:c.1861+124A>G MANE Select	NP_000199.2:n.1861+124A>G
NM_001079817.3:c.1861+124A>G	NP_001073285.1:n.1861+124A>G