Canonical Allele Identifier: CA2587920851

Gene: INSR

Linked Data

• gnomAD v4: 19-7116886-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116886A>C , CM000681.2:g.7116886A>C	GRCh38
NC_000019.9:g.7116897A>C , CM000681.1:g.7116897A>C	GRCh37
NC_000019.8:g.7067897A>C	NCBI36
NG_008852.2:g.182115T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.*170T>G MANE Select	ENSP00000303830.4:n.*170T>G
ENST00000302850.9:c.*170T>G	ENSP00000303830.4:n.*170T>G
ENST00000341500.9:c.*170T>G	ENSP00000342838.4:n.*170T>G
NM_000208.2:c.*170T>G	NP_000199.2:n.*170T>G
NM_000208.3:c.*170T>G	NP_000199.2:n.*170T>G
NM_001079817.1:c.*170T>G	NP_001073285.1:n.*170T>G
NM_001079817.2:c.*170T>G	NP_001073285.1:n.*170T>G
XM_011527988.1:c.*170T>G	XP_011526290.1:n.*170T>G
XM_011527989.1:c.*170T>G	XP_011526291.1:n.*170T>G
XM_011527988.2:c.*170T>G	XP_011526290.2:n.*170T>G
XM_011527989.3:c.*170T>G	XP_011526291.2:n.*170T>G
NM_000208.4:c.*170T>G MANE Select	NP_000199.2:n.*170T>G
NM_001079817.3:c.*170T>G	NP_001073285.1:n.*170T>G