Canonical Allele Identifier: CA505217404

Gene: INSR

Linked Data

• dbSNP Id: rs1972710958
• gnomAD v3: 19-7128914-G-T
• gnomAD v4: 19-7128914-G-T
• MyVariant Identifiers: chr19:g.7128925G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128914G>T , CM000681.2:g.7128914G>T	GRCh38
NC_000019.9:g.7128925G>T , CM000681.1:g.7128925G>T	GRCh37
NC_000019.8:g.7079925G>T	NCBI36
NG_008852.2:g.170087C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2883C>A MANE Select	ENSP00000303830.4:p.Pro961=
ENST00000302850.9:c.2883C>A	ENSP00000303830.4:p.Pro961=
ENST00000341500.9:c.2847C>A	ENSP00000342838.4:p.Pro949=
NM_000208.2:c.2883C>A	NP_000199.2:p.Pro961=
NM_000208.3:c.2883C>A	NP_000199.2:p.Pro961=
NM_001079817.1:c.2847C>A	NP_001073285.1:p.Pro949=
NM_001079817.2:c.2847C>A	NP_001073285.1:p.Pro949=
XM_011527988.1:c.2958C>A	XP_011526290.1:p.Pro986=
XM_011527989.1:c.2922C>A	XP_011526291.1:p.Pro974=
XM_011527988.2:c.2880C>A	XP_011526290.2:p.Pro960=
XM_011527989.3:c.2844C>A	XP_011526291.2:p.Pro948=
NM_000208.4:c.2883C>A MANE Select	NP_000199.2:p.Pro961=
NM_001079817.3:c.2847C>A	NP_001073285.1:p.Pro949=