Canonical Allele Identifier: CA631690931

Gene: INSR

Linked Data

• gnomAD v2: 19-7166043-TAAA-T
• gnomAD v3: 19-7166032-TAAA-T
• gnomAD v4: 19-7166032-TAAA-T
• MyVariant Identifiers: chr19:g.7166044_7166046del (hg19) ; chr19:g.7166033_7166035del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166045_7166047del , CM000681.2:g.7166045_7166047del	GRCh38
NC_000019.9:g.7166056_7166058del , CM000681.1:g.7166056_7166058del	GRCh37
NC_000019.8:g.7117056_7117058del	NCBI36
NG_008852.2:g.132966_132968del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.1861+119_1861+121del MANE Select	ENSP00000303830.4:n.1861+119_1861+121del
ENST00000302850.9:c.1861+119_1861+121del	ENSP00000303830.4:n.1861+119_1861+121del
ENST00000341500.9:c.1861+119_1861+121del	ENSP00000342838.4:n.1861+119_1861+121del
ENST00000598216.1:n.1836+119_1836+121del
ENST00000600492.1:c.262+119_262+121del	ENSP00000473170.1:n.262+119_262+121del
NM_000208.2:c.1861+119_1861+121del	NP_000199.2:n.1861+119_1861+121del
NM_000208.3:c.1861+119_1861+121del	NP_000199.2:n.1861+119_1861+121del
NM_001079817.1:c.1861+119_1861+121del	NP_001073285.1:n.1861+119_1861+121del
NM_001079817.2:c.1861+119_1861+121del	NP_001073285.1:n.1861+119_1861+121del
XM_011527988.1:c.1939+119_1939+121del	XP_011526290.1:n.1939+119_1939+121del
XM_011527989.1:c.1939+119_1939+121del	XP_011526291.1:n.1939+119_1939+121del
XM_011527988.2:c.1861+119_1861+121del	XP_011526290.2:n.1861+119_1861+121del
XM_011527989.3:c.1861+119_1861+121del	XP_011526291.2:n.1861+119_1861+121del
NM_000208.4:c.1861+119_1861+121del MANE Select	NP_000199.2:n.1861+119_1861+121del
NM_001079817.3:c.1861+119_1861+121del	NP_001073285.1:n.1861+119_1861+121del