Canonical Allele Identifier: CA505400048

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117191del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117185del , CM000681.2:g.7117185del	GRCh38
NC_000019.9:g.7117196del , CM000681.1:g.7117196del	GRCh37
NC_000019.8:g.7068196del	NCBI36
NG_008852.2:g.181821del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4025del MANE Select	ENSP00000303830.4:p.Gly1342AlafsTer23
ENST00000302850.9:c.4025del	ENSP00000303830.4:p.Gly1342AlafsTer23
ENST00000341500.9:c.3989del	ENSP00000342838.4:p.Gly1330AlafsTer23
NM_000208.2:c.4025del	NP_000199.2:p.Gly1342AlafsTer23
NM_000208.3:c.4025del	NP_000199.2:p.Gly1342AlafsTer23
NM_001079817.1:c.3989del	NP_001073285.1:p.Gly1330AlafsTer23
NM_001079817.2:c.3989del	NP_001073285.1:p.Gly1330AlafsTer23
XM_011527988.1:c.4100del	XP_011526290.1:p.Gly1367AlafsTer23
XM_011527989.1:c.4064del	XP_011526291.1:p.Gly1355AlafsTer23
XM_011527988.2:c.4022del	XP_011526290.2:p.Gly1341AlafsTer23
XM_011527989.3:c.3986del	XP_011526291.2:p.Gly1329AlafsTer23
NM_000208.4:c.4025del MANE Select	NP_000199.2:p.Gly1342AlafsTer23
NM_001079817.3:c.3989del	NP_001073285.1:p.Gly1330AlafsTer23