Canonical Allele Identifier: CA2587926320

Gene: INSR

Linked Data

• gnomAD v4: 19-7184653-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184654_7184655insAA , CM000681.2:g.7184654_7184655insAA	GRCh38
NC_000019.9:g.7184665_7184666insAA , CM000681.1:g.7184665_7184666insAA	GRCh37
NC_000019.8:g.7135665_7135666insAA	NCBI36
NG_008852.2:g.114347_114348insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-17_653-16insTT MANE Select	ENSP00000303830.4:n.653-17_653-16insTT
ENST00000302850.9:c.653-17_653-16insTT	ENSP00000303830.4:n.653-17_653-16insTT
ENST00000341500.9:c.653-17_653-16insTT	ENSP00000342838.4:n.653-17_653-16insTT
ENST00000598216.1:n.628-17_628-16insTT
NM_000208.2:c.653-17_653-16insTT	NP_000199.2:n.653-17_653-16insTT
NM_000208.3:c.653-17_653-16insTT	NP_000199.2:n.653-17_653-16insTT
NM_001079817.1:c.653-17_653-16insTT	NP_001073285.1:n.653-17_653-16insTT
NM_001079817.2:c.653-17_653-16insTT	NP_001073285.1:n.653-17_653-16insTT
XM_011527988.1:c.731-17_731-16insTT	XP_011526290.1:n.731-17_731-16insTT
XM_011527989.1:c.731-17_731-16insTT	XP_011526291.1:n.731-17_731-16insTT
XM_011527988.2:c.653-17_653-16insTT	XP_011526290.2:n.653-17_653-16insTT
XM_011527989.3:c.653-17_653-16insTT	XP_011526291.2:n.653-17_653-16insTT
NM_000208.4:c.653-17_653-16insTT MANE Select	NP_000199.2:n.653-17_653-16insTT
NM_001079817.3:c.653-17_653-16insTT	NP_001073285.1:n.653-17_653-16insTT