Canonical Allele Identifier: CA505216672

Gene: INSR

Linked Data

• gnomAD v4: 19-7120678-G-T
• MyVariant Identifiers: chr19:g.7120689G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120678G>T , CM000681.2:g.7120678G>T	GRCh38
NC_000019.9:g.7120689G>T , CM000681.1:g.7120689G>T	GRCh37
NC_000019.8:g.7071689G>T	NCBI36
NG_008852.2:g.178323C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3601C>A MANE Select	ENSP00000303830.4:p.Arg1201=
ENST00000302850.9:c.3601C>A	ENSP00000303830.4:p.Arg1201=
ENST00000341500.9:c.3565C>A	ENSP00000342838.4:p.Arg1189=
ENST00000601099.1:n.512C>A
NM_000208.2:c.3601C>A	NP_000199.2:p.Arg1201=
NM_000208.3:c.3601C>A	NP_000199.2:p.Arg1201=
NM_001079817.1:c.3565C>A	NP_001073285.1:p.Arg1189=
NM_001079817.2:c.3565C>A	NP_001073285.1:p.Arg1189=
XM_011527988.1:c.3676C>A	XP_011526290.1:p.Arg1226=
XM_011527989.1:c.3640C>A	XP_011526291.1:p.Arg1214=
XM_011527988.2:c.3598C>A	XP_011526290.2:p.Arg1200=
XM_011527989.3:c.3562C>A	XP_011526291.2:p.Arg1188=
NM_000208.4:c.3601C>A MANE Select	NP_000199.2:p.Arg1201=
NM_001079817.3:c.3565C>A	NP_001073285.1:p.Arg1189=