Canonical Allele Identifier: CA2320771033

Gene: INSR

Linked Data

• dbSNP Id: rs1568434377
• gnomAD v4: 19-7132123-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132123A>G , CM000681.2:g.7132123A>G	GRCh38
NC_000019.9:g.7132134A>G , CM000681.1:g.7132134A>G	GRCh37
NC_000019.8:g.7083134A>G	NCBI36
NG_008852.2:g.166878T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2842+35T>C MANE Select	ENSP00000303830.4:n.2842+35T>C
ENST00000302850.9:c.2842+35T>C	ENSP00000303830.4:n.2842+35T>C
ENST00000341500.9:c.2806+35T>C	ENSP00000342838.4:n.2806+35T>C
NM_000208.2:c.2842+35T>C	NP_000199.2:n.2842+35T>C
NM_000208.3:c.2842+35T>C	NP_000199.2:n.2842+35T>C
NM_001079817.1:c.2806+35T>C	NP_001073285.1:n.2806+35T>C
NM_001079817.2:c.2806+35T>C	NP_001073285.1:n.2806+35T>C
XM_011527988.1:c.2920+35T>C	XP_011526290.1:n.2920+35T>C
XM_011527989.1:c.2884+35T>C	XP_011526291.1:n.2884+35T>C
XM_011527988.2:c.2842+35T>C	XP_011526290.2:n.2842+35T>C
XM_011527989.3:c.2806+35T>C	XP_011526291.2:n.2806+35T>C
NM_000208.4:c.2842+35T>C MANE Select	NP_000199.2:n.2842+35T>C
NM_001079817.3:c.2806+35T>C	NP_001073285.1:n.2806+35T>C