Canonical Allele Identifier: CA403670815

Gene: INSR

Linked Data

• gnomAD v4: 19-7122924-G-T
• MyVariant Identifiers: chr19:g.7122935G>T (hg19) ; chr19:g.7122924G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122924G>T , CM000681.2:g.7122924G>T	GRCh38
NC_000019.9:g.7122935G>T , CM000681.1:g.7122935G>T	GRCh37
NC_000019.8:g.7073935G>T	NCBI36
NG_008852.2:g.176077C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3324C>A MANE Select	ENSP00000303830.4:p.His1108Gln
ENST00000302850.9:c.3324C>A	ENSP00000303830.4:p.His1108Gln
ENST00000341500.9:c.3288C>A	ENSP00000342838.4:p.His1096Gln
ENST00000593970.1:n.170C>A
ENST00000601099.1:n.235C>A
NM_000208.2:c.3324C>A	NP_000199.2:p.His1108Gln
NM_000208.3:c.3324C>A	NP_000199.2:p.His1108Gln
NM_001079817.1:c.3288C>A	NP_001073285.1:p.His1096Gln
NM_001079817.2:c.3288C>A	NP_001073285.1:p.His1096Gln
XM_011527988.1:c.3399C>A	XP_011526290.1:p.His1133Gln
XM_011527989.1:c.3363C>A	XP_011526291.1:p.His1121Gln
XM_011527988.2:c.3321C>A	XP_011526290.2:p.His1107Gln
XM_011527989.3:c.3285C>A	XP_011526291.2:p.His1095Gln
NM_000208.4:c.3324C>A MANE Select	NP_000199.2:p.His1108Gln
NM_001079817.3:c.3288C>A	NP_001073285.1:p.His1096Gln