Canonical Allele Identifier: CA884184594

Gene: INSR

Linked Data

• dbSNP Id: rs1277607083
• gnomAD v3: 19-7182994-G-GT
• gnomAD v4: 19-7182994-G-GT
• MyVariant Identifiers: chr19:g.7183005_7183006insT (hg19) ; chr19:g.7182994_7182995insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7183001dup , CM000681.2:g.7183001dup	GRCh38
NC_000019.9:g.7183012dup , CM000681.1:g.7183012dup	GRCh37
NC_000019.8:g.7134012dup	NCBI36
NG_008852.2:g.116006dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.974+1321dup MANE Select	ENSP00000303830.4:n.974+1321dup
ENST00000302850.9:c.974+1321dup	ENSP00000303830.4:n.974+1321dup
ENST00000341500.9:c.974+1321dup	ENSP00000342838.4:n.974+1321dup
ENST00000598216.1:n.949+1321dup
NM_000208.2:c.974+1321dup	NP_000199.2:n.974+1321dup
NM_000208.3:c.974+1321dup	NP_000199.2:n.974+1321dup
NM_001079817.1:c.974+1321dup	NP_001073285.1:n.974+1321dup
NM_001079817.2:c.974+1321dup	NP_001073285.1:n.974+1321dup
XM_011527988.1:c.1052+1321dup	XP_011526290.1:n.1052+1321dup
XM_011527989.1:c.1052+1321dup	XP_011526291.1:n.1052+1321dup
XM_011527988.2:c.974+1321dup	XP_011526290.2:n.974+1321dup
XM_011527989.3:c.974+1321dup	XP_011526291.2:n.974+1321dup
NM_000208.4:c.974+1321dup MANE Select	NP_000199.2:n.974+1321dup
NM_001079817.3:c.974+1321dup	NP_001073285.1:n.974+1321dup