Canonical Allele Identifier: CA884196579

Gene: INSR

Linked Data

• dbSNP Id: rs1490744146
• gnomAD v3: 19-7211675-G-GCAGTTTA
• gnomAD v4: 19-7211675-G-GCAGTTTA
• MyVariant Identifiers: chr19:g.7211686_7211687insCAGTTTA (hg19) ; chr19:g.7211675_7211676insCAGTTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7211676_7211677insAGTTTAC , CM000681.2:g.7211676_7211677insAGTTTAC	GRCh38
NC_000019.9:g.7211687_7211688insAGTTTAC , CM000681.1:g.7211687_7211688insAGTTTAC	GRCh37
NC_000019.8:g.7162687_7162688insAGTTTAC	NCBI36
NG_008852.2:g.87325_87326insTAAACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27039_653-27038insTAAACTG MANE Select	ENSP00000303830.4:n.653-27039_653-27038insTAAACTG
ENST00000302850.9:c.653-27039_653-27038insTAAACTG	ENSP00000303830.4:n.653-27039_653-27038insTAAACTG
ENST00000341500.9:c.653-27039_653-27038insTAAACTG	ENSP00000342838.4:n.653-27039_653-27038insTAAACTG
ENST00000598216.1:n.628-27039_628-27038insTAAACTG
NM_000208.2:c.653-27039_653-27038insTAAACTG	NP_000199.2:n.653-27039_653-27038insTAAACTG
NM_000208.3:c.653-27039_653-27038insTAAACTG	NP_000199.2:n.653-27039_653-27038insTAAACTG
NM_001079817.1:c.653-27039_653-27038insTAAACTG	NP_001073285.1:n.653-27039_653-27038insTAAACTG
NM_001079817.2:c.653-27039_653-27038insTAAACTG	NP_001073285.1:n.653-27039_653-27038insTAAACTG
XM_011527988.1:c.731-27039_731-27038insTAAACTG	XP_011526290.1:n.731-27039_731-27038insTAAACTG
XM_011527989.1:c.731-27039_731-27038insTAAACTG	XP_011526291.1:n.731-27039_731-27038insTAAACTG
XM_011527988.2:c.653-27039_653-27038insTAAACTG	XP_011526290.2:n.653-27039_653-27038insTAAACTG
XM_011527989.3:c.653-27039_653-27038insTAAACTG	XP_011526291.2:n.653-27039_653-27038insTAAACTG
NM_000208.4:c.653-27039_653-27038insTAAACTG MANE Select	NP_000199.2:n.653-27039_653-27038insTAAACTG
NM_001079817.3:c.653-27039_653-27038insTAAACTG	NP_001073285.1:n.653-27039_653-27038insTAAACTG