Canonical Allele Identifier: CA505400448

Gene: INSR

Linked Data

• gnomAD v4: 19-7143075-G-A
• MyVariant Identifiers: chr19:g.7143086G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7143075G>A , CM000681.2:g.7143075G>A	GRCh38
NC_000019.9:g.7143086G>A , CM000681.1:g.7143086G>A	GRCh37
NC_000019.8:g.7094086G>A	NCBI36
NG_008852.2:g.155926C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2283C>T MANE Select	ENSP00000303830.4:p.Arg761=
ENST00000302850.9:c.2283C>T	ENSP00000303830.4:p.Arg761=
ENST00000341500.9:c.2247C>T	ENSP00000342838.4:p.Arg749=
NM_000208.2:c.2283C>T	NP_000199.2:p.Arg761=
NM_000208.3:c.2283C>T	NP_000199.2:p.Arg761=
NM_001079817.1:c.2247C>T	NP_001073285.1:p.Arg749=
NM_001079817.2:c.2247C>T	NP_001073285.1:p.Arg749=
XM_011527988.1:c.2361C>T	XP_011526290.1:p.Arg787=
XM_011527989.1:c.2325C>T	XP_011526291.1:p.Arg775=
XM_011527988.2:c.2283C>T	XP_011526290.2:p.Arg761=
XM_011527989.3:c.2247C>T	XP_011526291.2:p.Arg749=
NM_000208.4:c.2283C>T MANE Select	NP_000199.2:p.Arg761=
NM_001079817.3:c.2247C>T	NP_001073285.1:p.Arg749=