Canonical Allele Identifier: CA505400097

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117289G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117278G>A , CM000681.2:g.7117278G>A	GRCh38
NC_000019.9:g.7117289G>A , CM000681.1:g.7117289G>A	GRCh37
NC_000019.8:g.7068289G>A	NCBI36
NG_008852.2:g.181723C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3927C>T MANE Select	ENSP00000303830.4:p.Asn1309=
ENST00000302850.9:c.3927C>T	ENSP00000303830.4:p.Asn1309=
ENST00000341500.9:c.3891C>T	ENSP00000342838.4:p.Asn1297=
NM_000208.2:c.3927C>T	NP_000199.2:p.Asn1309=
NM_000208.3:c.3927C>T	NP_000199.2:p.Asn1309=
NM_001079817.1:c.3891C>T	NP_001073285.1:p.Asn1297=
NM_001079817.2:c.3891C>T	NP_001073285.1:p.Asn1297=
XM_011527988.1:c.4002C>T	XP_011526290.1:p.Asn1334=
XM_011527989.1:c.3966C>T	XP_011526291.1:p.Asn1322=
XM_011527988.2:c.3924C>T	XP_011526290.2:p.Asn1308=
XM_011527989.3:c.3888C>T	XP_011526291.2:p.Asn1296=
NM_000208.4:c.3927C>T MANE Select	NP_000199.2:p.Asn1309=
NM_001079817.3:c.3891C>T	NP_001073285.1:p.Asn1297=