Canonical Allele Identifier: CA2587922466

Gene: INSR

Linked Data

• gnomAD v4: 19-7128800-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128805del , CM000681.2:g.7128805del	GRCh38
NC_000019.9:g.7128816del , CM000681.1:g.7128816del	GRCh37
NC_000019.8:g.7079816del	NCBI36
NG_008852.2:g.170200del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2945+51del MANE Select	ENSP00000303830.4:n.2945+51del
ENST00000302850.9:c.2945+51del	ENSP00000303830.4:n.2945+51del
ENST00000341500.9:c.2909+51del	ENSP00000342838.4:n.2909+51del
NM_000208.2:c.2945+51del	NP_000199.2:n.2945+51del
NM_000208.3:c.2945+51del	NP_000199.2:n.2945+51del
NM_001079817.1:c.2909+51del	NP_001073285.1:n.2909+51del
NM_001079817.2:c.2909+51del	NP_001073285.1:n.2909+51del
XM_011527988.1:c.3020+51del	XP_011526290.1:n.3020+51del
XM_011527989.1:c.2984+51del	XP_011526291.1:n.2984+51del
XM_011527988.2:c.2942+51del	XP_011526290.2:n.2942+51del
XM_011527989.3:c.2906+51del	XP_011526291.2:n.2906+51del
NM_000208.4:c.2945+51del MANE Select	NP_000199.2:n.2945+51del
NM_001079817.3:c.2909+51del	NP_001073285.1:n.2909+51del