Canonical Allele Identifier: CA2587926159

Gene: INSR

Linked Data

• gnomAD v4: 19-7184234-G-GAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184234_7184235insAGT , CM000681.2:g.7184234_7184235insAGT	GRCh38
NC_000019.9:g.7184245_7184246insAGT , CM000681.1:g.7184245_7184246insAGT	GRCh37
NC_000019.8:g.7135245_7135246insAGT	NCBI36
NG_008852.2:g.114766_114767insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.974+81_974+82insACT MANE Select	ENSP00000303830.4:n.974+81_974+82insACT
ENST00000302850.9:c.974+81_974+82insACT	ENSP00000303830.4:n.974+81_974+82insACT
ENST00000341500.9:c.974+81_974+82insACT	ENSP00000342838.4:n.974+81_974+82insACT
ENST00000598216.1:n.949+81_949+82insACT
NM_000208.2:c.974+81_974+82insACT	NP_000199.2:n.974+81_974+82insACT
NM_000208.3:c.974+81_974+82insACT	NP_000199.2:n.974+81_974+82insACT
NM_001079817.1:c.974+81_974+82insACT	NP_001073285.1:n.974+81_974+82insACT
NM_001079817.2:c.974+81_974+82insACT	NP_001073285.1:n.974+81_974+82insACT
XM_011527988.1:c.1052+81_1052+82insACT	XP_011526290.1:n.1052+81_1052+82insACT
XM_011527989.1:c.1052+81_1052+82insACT	XP_011526291.1:n.1052+81_1052+82insACT
XM_011527988.2:c.974+81_974+82insACT	XP_011526290.2:n.974+81_974+82insACT
XM_011527989.3:c.974+81_974+82insACT	XP_011526291.2:n.974+81_974+82insACT
NM_000208.4:c.974+81_974+82insACT MANE Select	NP_000199.2:n.974+81_974+82insACT
NM_001079817.3:c.974+81_974+82insACT	NP_001073285.1:n.974+81_974+82insACT