Canonical Allele Identifier: CA403672180

Gene: INSR

Linked Data

• dbSNP Id: rs753474375
• gnomAD v2: 19-7132306-C-A
• gnomAD v4: 19-7132295-C-A
• MyVariant Identifiers: chr19:g.7132306C>A (hg19) ; chr19:g.7132295C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132295C>A , CM000681.2:g.7132295C>A	GRCh38
NC_000019.9:g.7132306C>A , CM000681.1:g.7132306C>A	GRCh37
NC_000019.8:g.7083306C>A	NCBI36
NG_008852.2:g.166706G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2705G>T MANE Select	ENSP00000303830.4:p.Arg902Leu
ENST00000302850.9:c.2705G>T	ENSP00000303830.4:p.Arg902Leu
ENST00000341500.9:c.2669G>T	ENSP00000342838.4:p.Arg890Leu
NM_000208.2:c.2705G>T	NP_000199.2:p.Arg902Leu
NM_000208.3:c.2705G>T	NP_000199.2:p.Arg902Leu
NM_001079817.1:c.2669G>T	NP_001073285.1:p.Arg890Leu
NM_001079817.2:c.2669G>T	NP_001073285.1:p.Arg890Leu
XM_011527988.1:c.2783G>T	XP_011526290.1:p.Arg928Leu
XM_011527989.1:c.2747G>T	XP_011526291.1:p.Arg916Leu
XM_011527988.2:c.2705G>T	XP_011526290.2:p.Arg902Leu
XM_011527989.3:c.2669G>T	XP_011526291.2:p.Arg890Leu
NM_000208.4:c.2705G>T MANE Select	NP_000199.2:p.Arg902Leu
NM_001079817.3:c.2669G>T	NP_001073285.1:p.Arg890Leu