Canonical Allele Identifier: CA2320795488

Gene: INSR

Linked Data

• dbSNP Id: rs1974317229

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7183095A>T , CM000681.2:g.7183095A>T	GRCh38
NC_000019.9:g.7183106A>T , CM000681.1:g.7183106A>T	GRCh37
NC_000019.8:g.7134106A>T	NCBI36
NG_008852.2:g.115906T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.974+1221T>A MANE Select	ENSP00000303830.4:n.974+1221T>A
ENST00000302850.9:c.974+1221T>A	ENSP00000303830.4:n.974+1221T>A
ENST00000341500.9:c.974+1221T>A	ENSP00000342838.4:n.974+1221T>A
ENST00000598216.1:n.949+1221T>A
NM_000208.2:c.974+1221T>A	NP_000199.2:n.974+1221T>A
NM_000208.3:c.974+1221T>A	NP_000199.2:n.974+1221T>A
NM_001079817.1:c.974+1221T>A	NP_001073285.1:n.974+1221T>A
NM_001079817.2:c.974+1221T>A	NP_001073285.1:n.974+1221T>A
XM_011527988.1:c.1052+1221T>A	XP_011526290.1:n.1052+1221T>A
XM_011527989.1:c.1052+1221T>A	XP_011526291.1:n.1052+1221T>A
XM_011527988.2:c.974+1221T>A	XP_011526290.2:n.974+1221T>A
XM_011527989.3:c.974+1221T>A	XP_011526291.2:n.974+1221T>A
NM_000208.4:c.974+1221T>A MANE Select	NP_000199.2:n.974+1221T>A
NM_001079817.3:c.974+1221T>A	NP_001073285.1:n.974+1221T>A