Canonical Allele Identifier: CA993111834

Gene: INSR

Linked Data

• dbSNP Id: rs1973879121
• gnomAD v3: 19-7165977-CA-C
• gnomAD v4: 19-7165977-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7165978del , CM000681.2:g.7165978del	GRCh38
NC_000019.9:g.7165989del , CM000681.1:g.7165989del	GRCh37
NC_000019.8:g.7116989del	NCBI36
NG_008852.2:g.133023del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1861+176del MANE Select	ENSP00000303830.4:n.1861+176del
ENST00000302850.9:c.1861+176del	ENSP00000303830.4:n.1861+176del
ENST00000341500.9:c.1861+176del	ENSP00000342838.4:n.1861+176del
ENST00000598216.1:n.1836+176del
ENST00000600492.1:c.262+176del	ENSP00000473170.1:n.262+176del
NM_000208.2:c.1861+176del	NP_000199.2:n.1861+176del
NM_000208.3:c.1861+176del	NP_000199.2:n.1861+176del
NM_001079817.1:c.1861+176del	NP_001073285.1:n.1861+176del
NM_001079817.2:c.1861+176del	NP_001073285.1:n.1861+176del
XM_011527988.1:c.1939+176del	XP_011526290.1:n.1939+176del
XM_011527989.1:c.1939+176del	XP_011526291.1:n.1939+176del
XM_011527988.2:c.1861+176del	XP_011526290.2:n.1861+176del
XM_011527989.3:c.1861+176del	XP_011526291.2:n.1861+176del
NM_000208.4:c.1861+176del MANE Select	NP_000199.2:n.1861+176del
NM_001079817.3:c.1861+176del	NP_001073285.1:n.1861+176del