Canonical Allele Identifier: CA993107781

Gene: INSR

Linked Data

• dbSNP Id: rs1972716907
• gnomAD v3: 19-7129114-AG-A
• gnomAD v4: 19-7129114-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7129115del , CM000681.2:g.7129115del	GRCh38
NC_000019.9:g.7129126del , CM000681.1:g.7129126del	GRCh37
NC_000019.8:g.7080126del	NCBI36
NG_008852.2:g.169886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2843-161del MANE Select	ENSP00000303830.4:n.2843-161del
ENST00000302850.9:c.2843-161del	ENSP00000303830.4:n.2843-161del
ENST00000341500.9:c.2807-161del	ENSP00000342838.4:n.2807-161del
NM_000208.2:c.2843-161del	NP_000199.2:n.2843-161del
NM_000208.3:c.2843-161del	NP_000199.2:n.2843-161del
NM_001079817.1:c.2807-161del	NP_001073285.1:n.2807-161del
NM_001079817.2:c.2807-161del	NP_001073285.1:n.2807-161del
XM_011527988.1:c.2921-164del	XP_011526290.1:n.2921-164del
XM_011527989.1:c.2885-164del	XP_011526291.1:n.2885-164del
XM_011527988.2:c.2843-164del	XP_011526290.2:n.2843-164del
XM_011527989.3:c.2807-164del	XP_011526291.2:n.2807-164del
NM_000208.4:c.2843-161del MANE Select	NP_000199.2:n.2843-161del
NM_001079817.3:c.2807-161del	NP_001073285.1:n.2807-161del