Canonical Allele Identifier: CA631690926

Gene: INSR

Linked Data

• dbSNP Id: rs1973880504
• gnomAD v2: 19-7166042-C-CA
• gnomAD v3: 19-7166031-C-CA
• gnomAD v4: 19-7166031-C-CA
• MyVariant Identifiers: chr19:g.7166042_7166043insA (hg19) ; chr19:g.7166031_7166032insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166031_7166032insA , CM000681.2:g.7166031_7166032insA	GRCh38
NC_000019.9:g.7166042_7166043insA , CM000681.1:g.7166042_7166043insA	GRCh37
NC_000019.8:g.7117042_7117043insA	NCBI36
NG_008852.2:g.132969_132970insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1861+122_1861+123insT MANE Select	ENSP00000303830.4:n.1861+122_1861+123insT
ENST00000302850.9:c.1861+122_1861+123insT	ENSP00000303830.4:n.1861+122_1861+123insT
ENST00000341500.9:c.1861+122_1861+123insT	ENSP00000342838.4:n.1861+122_1861+123insT
ENST00000598216.1:n.1836+122_1836+123insT
ENST00000600492.1:c.262+122_262+123insT	ENSP00000473170.1:n.262+122_262+123insT
NM_000208.2:c.1861+122_1861+123insT	NP_000199.2:n.1861+122_1861+123insT
NM_000208.3:c.1861+122_1861+123insT	NP_000199.2:n.1861+122_1861+123insT
NM_001079817.1:c.1861+122_1861+123insT	NP_001073285.1:n.1861+122_1861+123insT
NM_001079817.2:c.1861+122_1861+123insT	NP_001073285.1:n.1861+122_1861+123insT
XM_011527988.1:c.1939+122_1939+123insT	XP_011526290.1:n.1939+122_1939+123insT
XM_011527989.1:c.1939+122_1939+123insT	XP_011526291.1:n.1939+122_1939+123insT
XM_011527988.2:c.1861+122_1861+123insT	XP_011526290.2:n.1861+122_1861+123insT
XM_011527989.3:c.1861+122_1861+123insT	XP_011526291.2:n.1861+122_1861+123insT
NM_000208.4:c.1861+122_1861+123insT MANE Select	NP_000199.2:n.1861+122_1861+123insT
NM_001079817.3:c.1861+122_1861+123insT	NP_001073285.1:n.1861+122_1861+123insT