Canonical Allele Identifier: CA505400042

Gene: INSR

Linked Data

• gnomAD v4: 19-7117176-C-G
• MyVariant Identifiers: chr19:g.7117187C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117176C>G , CM000681.2:g.7117176C>G	GRCh38
NC_000019.9:g.7117187C>G , CM000681.1:g.7117187C>G	GRCh37
NC_000019.8:g.7068187C>G	NCBI36
NG_008852.2:g.181825G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4029G>C MANE Select	ENSP00000303830.4:p.Arg1343=
ENST00000302850.9:c.4029G>C	ENSP00000303830.4:p.Arg1343=
ENST00000341500.9:c.3993G>C	ENSP00000342838.4:p.Arg1331=
NM_000208.2:c.4029G>C	NP_000199.2:p.Arg1343=
NM_000208.3:c.4029G>C	NP_000199.2:p.Arg1343=
NM_001079817.1:c.3993G>C	NP_001073285.1:p.Arg1331=
NM_001079817.2:c.3993G>C	NP_001073285.1:p.Arg1331=
XM_011527988.1:c.4104G>C	XP_011526290.1:p.Arg1368=
XM_011527989.1:c.4068G>C	XP_011526291.1:p.Arg1356=
XM_011527988.2:c.4026G>C	XP_011526290.2:p.Arg1342=
XM_011527989.3:c.3990G>C	XP_011526291.2:p.Arg1330=
NM_000208.4:c.4029G>C MANE Select	NP_000199.2:p.Arg1343=
NM_001079817.3:c.3993G>C	NP_001073285.1:p.Arg1331=