Canonical Allele Identifier: CA993111888

Gene: INSR

Linked Data

• gnomAD v3: 19-7166029-GTCT-G
• gnomAD v4: 19-7166029-GTCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166030_7166032del , CM000681.2:g.7166030_7166032del	GRCh38
NC_000019.9:g.7166041_7166043del , CM000681.1:g.7166041_7166043del	GRCh37
NC_000019.8:g.7117041_7117043del	NCBI36
NG_008852.2:g.132969_132971del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.1861+122_1861+124del MANE Select	ENSP00000303830.4:n.1861+122_1861+124del
ENST00000302850.9:c.1861+122_1861+124del	ENSP00000303830.4:n.1861+122_1861+124del
ENST00000341500.9:c.1861+122_1861+124del	ENSP00000342838.4:n.1861+122_1861+124del
ENST00000598216.1:n.1836+122_1836+124del
ENST00000600492.1:c.262+122_262+124del	ENSP00000473170.1:n.262+122_262+124del
NM_000208.2:c.1861+122_1861+124del	NP_000199.2:n.1861+122_1861+124del
NM_000208.3:c.1861+122_1861+124del	NP_000199.2:n.1861+122_1861+124del
NM_001079817.1:c.1861+122_1861+124del	NP_001073285.1:n.1861+122_1861+124del
NM_001079817.2:c.1861+122_1861+124del	NP_001073285.1:n.1861+122_1861+124del
XM_011527988.1:c.1939+122_1939+124del	XP_011526290.1:n.1939+122_1939+124del
XM_011527989.1:c.1939+122_1939+124del	XP_011526291.1:n.1939+122_1939+124del
XM_011527988.2:c.1861+122_1861+124del	XP_011526290.2:n.1861+122_1861+124del
XM_011527989.3:c.1861+122_1861+124del	XP_011526291.2:n.1861+122_1861+124del
NM_000208.4:c.1861+122_1861+124del MANE Select	NP_000199.2:n.1861+122_1861+124del
NM_001079817.3:c.1861+122_1861+124del	NP_001073285.1:n.1861+122_1861+124del