Canonical Allele Identifier: CA2587922514

Gene: INSR

Linked Data

• gnomAD v4: 19-7129044-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7129044_7129045insC , CM000681.2:g.7129044_7129045insC	GRCh38
NC_000019.9:g.7129055_7129056insC , CM000681.1:g.7129055_7129056insC	GRCh37
NC_000019.8:g.7080055_7080056insC	NCBI36
NG_008852.2:g.169956_169957insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2843-91_2843-90insG MANE Select	ENSP00000303830.4:n.2843-91_2843-90insG
ENST00000302850.9:c.2843-91_2843-90insG	ENSP00000303830.4:n.2843-91_2843-90insG
ENST00000341500.9:c.2807-91_2807-90insG	ENSP00000342838.4:n.2807-91_2807-90insG
NM_000208.2:c.2843-91_2843-90insG	NP_000199.2:n.2843-91_2843-90insG
NM_000208.3:c.2843-91_2843-90insG	NP_000199.2:n.2843-91_2843-90insG
NM_001079817.1:c.2807-91_2807-90insG	NP_001073285.1:n.2807-91_2807-90insG
NM_001079817.2:c.2807-91_2807-90insG	NP_001073285.1:n.2807-91_2807-90insG
XM_011527988.1:c.2921-94_2921-93insG	XP_011526290.1:n.2921-94_2921-93insG
XM_011527989.1:c.2885-94_2885-93insG	XP_011526291.1:n.2885-94_2885-93insG
XM_011527988.2:c.2843-94_2843-93insG	XP_011526290.2:n.2843-94_2843-93insG
XM_011527989.3:c.2807-94_2807-93insG	XP_011526291.2:n.2807-94_2807-93insG
NM_000208.4:c.2843-91_2843-90insG MANE Select	NP_000199.2:n.2843-91_2843-90insG
NM_001079817.3:c.2807-91_2807-90insG	NP_001073285.1:n.2807-91_2807-90insG