Canonical Allele Identifier: CA505400170

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125312G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125301G>T , CM000681.2:g.7125301G>T	GRCh38
NC_000019.9:g.7125312G>T , CM000681.1:g.7125312G>T	GRCh37
NC_000019.8:g.7076312G>T	NCBI36
NG_008852.2:g.173700C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3240C>A MANE Select	ENSP00000303830.4:p.Gly1080=
ENST00000302850.9:c.3240C>A	ENSP00000303830.4:p.Gly1080=
ENST00000341500.9:c.3204C>A	ENSP00000342838.4:p.Gly1068=
ENST00000593970.1:n.86C>A
NM_000208.2:c.3240C>A	NP_000199.2:p.Gly1080=
NM_000208.3:c.3240C>A	NP_000199.2:p.Gly1080=
NM_001079817.1:c.3204C>A	NP_001073285.1:p.Gly1068=
NM_001079817.2:c.3204C>A	NP_001073285.1:p.Gly1068=
XM_011527988.1:c.3315C>A	XP_011526290.1:p.Gly1105=
XM_011527989.1:c.3279C>A	XP_011526291.1:p.Gly1093=
XM_011527988.2:c.3237C>A	XP_011526290.2:p.Gly1079=
XM_011527989.3:c.3201C>A	XP_011526291.2:p.Gly1067=
NM_000208.4:c.3240C>A MANE Select	NP_000199.2:p.Gly1080=
NM_001079817.3:c.3204C>A	NP_001073285.1:p.Gly1068=