Canonical Allele Identifier: CA403668799

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117341T>A (hg19) ; chr19:g.7117330T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117330T>A , CM000681.2:g.7117330T>A	GRCh38
NC_000019.9:g.7117341T>A , CM000681.1:g.7117341T>A	GRCh37
NC_000019.8:g.7068341T>A	NCBI36
NG_008852.2:g.181671A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3875A>T MANE Select	ENSP00000303830.4:p.Asp1292Val
ENST00000302850.9:c.3875A>T	ENSP00000303830.4:p.Asp1292Val
ENST00000341500.9:c.3839A>T	ENSP00000342838.4:p.Asp1280Val
NM_000208.2:c.3875A>T	NP_000199.2:p.Asp1292Val
NM_000208.3:c.3875A>T	NP_000199.2:p.Asp1292Val
NM_001079817.1:c.3839A>T	NP_001073285.1:p.Asp1280Val
NM_001079817.2:c.3839A>T	NP_001073285.1:p.Asp1280Val
XM_011527988.1:c.3950A>T	XP_011526290.1:p.Asp1317Val
XM_011527989.1:c.3914A>T	XP_011526291.1:p.Asp1305Val
XM_011527988.2:c.3872A>T	XP_011526290.2:p.Asp1291Val
XM_011527989.3:c.3836A>T	XP_011526291.2:p.Asp1279Val
NM_000208.4:c.3875A>T MANE Select	NP_000199.2:p.Asp1292Val
NM_001079817.3:c.3839A>T	NP_001073285.1:p.Asp1280Val