Canonical Allele Identifier: CA9135348

Gene: INSR

Linked Data

• dbSNP Id: rs376505773
• ExAC: 19:7125393 G / A
• gnomAD v2: 19-7125393-G-A
• gnomAD v3: 19-7125382-G-A
• gnomAD v4: 19-7125382-G-A
• COSMIC: COSM2728447 ; COSM2728448
• MyVariant Identifiers: chr19:g.7125393G>A (hg19) ; chr19:g.7125382G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125382G>A , CM000681.2:g.7125382G>A	GRCh38
NC_000019.9:g.7125393G>A , CM000681.1:g.7125393G>A	GRCh37
NC_000019.8:g.7076393G>A	NCBI36
NG_008852.2:g.173619C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3159C>T MANE Select	ENSP00000303830.4:p.Arg1053=
ENST00000302850.9:c.3159C>T	ENSP00000303830.4:p.Arg1053=
ENST00000341500.9:c.3123C>T	ENSP00000342838.4:p.Arg1041=
ENST00000593970.1:n.5C>T
NM_000208.2:c.3159C>T	NP_000199.2:p.Arg1053=
NM_000208.3:c.3159C>T	NP_000199.2:p.Arg1053=
NM_001079817.1:c.3123C>T	NP_001073285.1:p.Arg1041=
NM_001079817.2:c.3123C>T	NP_001073285.1:p.Arg1041=
XM_011527988.1:c.3234C>T	XP_011526290.1:p.Arg1078=
XM_011527989.1:c.3198C>T	XP_011526291.1:p.Arg1066=
XM_011527988.2:c.3156C>T	XP_011526290.2:p.Arg1052=
XM_011527989.3:c.3120C>T	XP_011526291.2:p.Arg1040=
NM_000208.4:c.3159C>T MANE Select	NP_000199.2:p.Arg1053=
NM_001079817.3:c.3123C>T	NP_001073285.1:p.Arg1041=