Canonical Allele Identifier: CA2587925139

Gene: INSR

Linked Data

• gnomAD v4: 19-7166037-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166037_7166038insT , CM000681.2:g.7166037_7166038insT	GRCh38
NC_000019.9:g.7166048_7166049insT , CM000681.1:g.7166048_7166049insT	GRCh37
NC_000019.8:g.7117048_7117049insT	NCBI36
NG_008852.2:g.132963_132964insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1861+116_1861+117insA MANE Select	ENSP00000303830.4:n.1861+116_1861+117insA
ENST00000302850.9:c.1861+116_1861+117insA	ENSP00000303830.4:n.1861+116_1861+117insA
ENST00000341500.9:c.1861+116_1861+117insA	ENSP00000342838.4:n.1861+116_1861+117insA
ENST00000598216.1:n.1836+116_1836+117insA
ENST00000600492.1:c.262+116_262+117insA	ENSP00000473170.1:n.262+116_262+117insA
NM_000208.2:c.1861+116_1861+117insA	NP_000199.2:n.1861+116_1861+117insA
NM_000208.3:c.1861+116_1861+117insA	NP_000199.2:n.1861+116_1861+117insA
NM_001079817.1:c.1861+116_1861+117insA	NP_001073285.1:n.1861+116_1861+117insA
NM_001079817.2:c.1861+116_1861+117insA	NP_001073285.1:n.1861+116_1861+117insA
XM_011527988.1:c.1939+116_1939+117insA	XP_011526290.1:n.1939+116_1939+117insA
XM_011527989.1:c.1939+116_1939+117insA	XP_011526291.1:n.1939+116_1939+117insA
XM_011527988.2:c.1861+116_1861+117insA	XP_011526290.2:n.1861+116_1861+117insA
XM_011527989.3:c.1861+116_1861+117insA	XP_011526291.2:n.1861+116_1861+117insA
NM_000208.4:c.1861+116_1861+117insA MANE Select	NP_000199.2:n.1861+116_1861+117insA
NM_001079817.3:c.1861+116_1861+117insA	NP_001073285.1:n.1861+116_1861+117insA