Canonical Allele Identifier: CA884184517

Gene: INSR

Linked Data

• dbSNP Id: rs1373182918
• gnomAD v2: 19-7182875-C-G
• gnomAD v3: 19-7182864-C-G
• gnomAD v4: 19-7182864-C-G
• MyVariant Identifiers: chr19:g.7182875C>G (hg19) ; chr19:g.7182864C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7182864C>G , CM000681.2:g.7182864C>G	GRCh38
NC_000019.9:g.7182875C>G , CM000681.1:g.7182875C>G	GRCh37
NC_000019.8:g.7133875C>G	NCBI36
NG_008852.2:g.116137G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.974+1452G>C MANE Select	ENSP00000303830.4:n.974+1452G>C
ENST00000302850.9:c.974+1452G>C	ENSP00000303830.4:n.974+1452G>C
ENST00000341500.9:c.974+1452G>C	ENSP00000342838.4:n.974+1452G>C
ENST00000598216.1:n.949+1452G>C
NM_000208.2:c.974+1452G>C	NP_000199.2:n.974+1452G>C
NM_000208.3:c.974+1452G>C	NP_000199.2:n.974+1452G>C
NM_001079817.1:c.974+1452G>C	NP_001073285.1:n.974+1452G>C
NM_001079817.2:c.974+1452G>C	NP_001073285.1:n.974+1452G>C
XM_011527988.1:c.1052+1452G>C	XP_011526290.1:n.1052+1452G>C
XM_011527989.1:c.1052+1452G>C	XP_011526291.1:n.1052+1452G>C
XM_011527988.2:c.974+1452G>C	XP_011526290.2:n.974+1452G>C
XM_011527989.3:c.974+1452G>C	XP_011526291.2:n.974+1452G>C
NM_000208.4:c.974+1452G>C MANE Select	NP_000199.2:n.974+1452G>C
NM_001079817.3:c.974+1452G>C	NP_001073285.1:n.974+1452G>C