Canonical Allele Identifier: CA9135421

Gene: INSR

Linked Data

• dbSNP Id: rs750365992
• ExAC: 19:7128931 G / A
• gnomAD v2: 19-7128931-G-A
• gnomAD v4: 19-7128920-G-A
• MyVariant Identifiers: chr19:g.7128931G>A (hg19) ; chr19:g.7128920G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128920G>A , CM000681.2:g.7128920G>A	GRCh38
NC_000019.9:g.7128931G>A , CM000681.1:g.7128931G>A	GRCh37
NC_000019.8:g.7079931G>A	NCBI36
NG_008852.2:g.170081C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2877C>T MANE Select	ENSP00000303830.4:p.Ile959=
ENST00000302850.9:c.2877C>T	ENSP00000303830.4:p.Ile959=
ENST00000341500.9:c.2841C>T	ENSP00000342838.4:p.Ile947=
NM_000208.2:c.2877C>T	NP_000199.2:p.Ile959=
NM_000208.3:c.2877C>T	NP_000199.2:p.Ile959=
NM_001079817.1:c.2841C>T	NP_001073285.1:p.Ile947=
NM_001079817.2:c.2841C>T	NP_001073285.1:p.Ile947=
XM_011527988.1:c.2952C>T	XP_011526290.1:p.Ile984=
XM_011527989.1:c.2916C>T	XP_011526291.1:p.Ile972=
XM_011527988.2:c.2874C>T	XP_011526290.2:p.Ile958=
XM_011527989.3:c.2838C>T	XP_011526291.2:p.Ile946=
NM_000208.4:c.2877C>T MANE Select	NP_000199.2:p.Ile959=
NM_001079817.3:c.2841C>T	NP_001073285.1:p.Ile947=