Canonical Allele Identifier: CA2587925847

Gene: INSR

Linked Data

• gnomAD v4: 19-7172554-CTCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7172559_7172561del , CM000681.2:g.7172559_7172561del	GRCh38
NC_000019.9:g.7172570_7172572del , CM000681.1:g.7172570_7172572del	GRCh37
NC_000019.8:g.7123570_7123572del	NCBI36
NG_008852.2:g.126444_126446del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1124-123_1124-121del MANE Select	ENSP00000303830.4:n.1124-123_1124-121del
ENST00000302850.9:c.1124-123_1124-121del	ENSP00000303830.4:n.1124-123_1124-121del
ENST00000341500.9:c.1124-123_1124-121del	ENSP00000342838.4:n.1124-123_1124-121del
ENST00000598216.1:n.1099-123_1099-121del
NM_000208.2:c.1124-123_1124-121del	NP_000199.2:n.1124-123_1124-121del
NM_000208.3:c.1124-123_1124-121del	NP_000199.2:n.1124-123_1124-121del
NM_001079817.1:c.1124-123_1124-121del	NP_001073285.1:n.1124-123_1124-121del
NM_001079817.2:c.1124-123_1124-121del	NP_001073285.1:n.1124-123_1124-121del
XM_011527988.1:c.1202-123_1202-121del	XP_011526290.1:n.1202-123_1202-121del
XM_011527989.1:c.1202-123_1202-121del	XP_011526291.1:n.1202-123_1202-121del
XM_011527988.2:c.1124-123_1124-121del	XP_011526290.2:n.1124-123_1124-121del
XM_011527989.3:c.1124-123_1124-121del	XP_011526291.2:n.1124-123_1124-121del
NM_000208.4:c.1124-123_1124-121del MANE Select	NP_000199.2:n.1124-123_1124-121del
NM_001079817.3:c.1124-123_1124-121del	NP_001073285.1:n.1124-123_1124-121del