Canonical Allele Identifier: CA9135558

Gene: INSR

Linked Data

• dbSNP Id: rs376600434
• ExAC: 19:7142989 C / G
• gnomAD v2: 19-7142989-C-G
• gnomAD v4: 19-7142978-C-G
• MyVariant Identifiers: chr19:g.7142989C>G (hg19) ; chr19:g.7142978C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7142978C>G , CM000681.2:g.7142978C>G	GRCh38
NC_000019.9:g.7142989C>G , CM000681.1:g.7142989C>G	GRCh37
NC_000019.8:g.7093989C>G	NCBI36
NG_008852.2:g.156023G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2380G>C MANE Select	ENSP00000303830.4:p.Glu794Gln
ENST00000302850.9:c.2380G>C	ENSP00000303830.4:p.Glu794Gln
ENST00000341500.9:c.2344G>C	ENSP00000342838.4:p.Glu782Gln
ENST00000597211.1:n.63G>C
NM_000208.2:c.2380G>C	NP_000199.2:p.Glu794Gln
NM_000208.3:c.2380G>C	NP_000199.2:p.Glu794Gln
NM_001079817.1:c.2344G>C	NP_001073285.1:p.Glu782Gln
NM_001079817.2:c.2344G>C	NP_001073285.1:p.Glu782Gln
XM_011527988.1:c.2458G>C	XP_011526290.1:p.Glu820Gln
XM_011527989.1:c.2422G>C	XP_011526291.1:p.Glu808Gln
XM_011527988.2:c.2380G>C	XP_011526290.2:p.Glu794Gln
XM_011527989.3:c.2344G>C	XP_011526291.2:p.Glu782Gln
NM_000208.4:c.2380G>C MANE Select	NP_000199.2:p.Glu794Gln
NM_001079817.3:c.2344G>C	NP_001073285.1:p.Glu782Gln