Canonical Allele Identifier: CA505217401

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128922G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128911G>T , CM000681.2:g.7128911G>T	GRCh38
NC_000019.9:g.7128922G>T , CM000681.1:g.7128922G>T	GRCh37
NC_000019.8:g.7079922G>T	NCBI36
NG_008852.2:g.170090C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2886C>A MANE Select	ENSP00000303830.4:p.Leu962=
ENST00000302850.9:c.2886C>A	ENSP00000303830.4:p.Leu962=
ENST00000341500.9:c.2850C>A	ENSP00000342838.4:p.Leu950=
NM_000208.2:c.2886C>A	NP_000199.2:p.Leu962=
NM_000208.3:c.2886C>A	NP_000199.2:p.Leu962=
NM_001079817.1:c.2850C>A	NP_001073285.1:p.Leu950=
NM_001079817.2:c.2850C>A	NP_001073285.1:p.Leu950=
XM_011527988.1:c.2961C>A	XP_011526290.1:p.Leu987=
XM_011527989.1:c.2925C>A	XP_011526291.1:p.Leu975=
XM_011527988.2:c.2883C>A	XP_011526290.2:p.Leu961=
XM_011527989.3:c.2847C>A	XP_011526291.2:p.Leu949=
NM_000208.4:c.2886C>A MANE Select	NP_000199.2:p.Leu962=
NM_001079817.3:c.2850C>A	NP_001073285.1:p.Leu950=