Canonical Allele Identifier: CA2320788343

Gene: INSR

Linked Data

• dbSNP Id: rs1599935391

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166511C>T , CM000681.2:g.7166511C>T	GRCh38
NC_000019.9:g.7166522C>T , CM000681.1:g.7166522C>T	GRCh37
NC_000019.8:g.7117522C>T	NCBI36
NG_008852.2:g.132490G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1611-107G>A MANE Select	ENSP00000303830.4:n.1611-107G>A
ENST00000302850.9:c.1611-107G>A	ENSP00000303830.4:n.1611-107G>A
ENST00000341500.9:c.1611-107G>A	ENSP00000342838.4:n.1611-107G>A
ENST00000598216.1:n.1586-107G>A
ENST00000600492.1:c.12-107G>A	ENSP00000473170.1:n.12-107G>A
NM_000208.2:c.1611-107G>A	NP_000199.2:n.1611-107G>A
NM_000208.3:c.1611-107G>A	NP_000199.2:n.1611-107G>A
NM_001079817.1:c.1611-107G>A	NP_001073285.1:n.1611-107G>A
NM_001079817.2:c.1611-107G>A	NP_001073285.1:n.1611-107G>A
XM_011527988.1:c.1689-107G>A	XP_011526290.1:n.1689-107G>A
XM_011527989.1:c.1689-107G>A	XP_011526291.1:n.1689-107G>A
XM_011527988.2:c.1611-107G>A	XP_011526290.2:n.1611-107G>A
XM_011527989.3:c.1611-107G>A	XP_011526291.2:n.1611-107G>A
NM_000208.4:c.1611-107G>A MANE Select	NP_000199.2:n.1611-107G>A
NM_001079817.3:c.1611-107G>A	NP_001073285.1:n.1611-107G>A