Canonical Allele Identifier: CA403671116

Gene: INSR

Linked Data

• gnomAD v4: 19-7125351-T-C
• MyVariant Identifiers: chr19:g.7125362T>C (hg19) ; chr19:g.7125351T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125351T>C , CM000681.2:g.7125351T>C	GRCh38
NC_000019.9:g.7125362T>C , CM000681.1:g.7125362T>C	GRCh37
NC_000019.8:g.7076362T>C	NCBI36
NG_008852.2:g.173650A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3190A>G MANE Select	ENSP00000303830.4:p.Ser1064Gly
ENST00000302850.9:c.3190A>G	ENSP00000303830.4:p.Ser1064Gly
ENST00000341500.9:c.3154A>G	ENSP00000342838.4:p.Ser1052Gly
ENST00000593970.1:n.36A>G
NM_000208.2:c.3190A>G	NP_000199.2:p.Ser1064Gly
NM_000208.3:c.3190A>G	NP_000199.2:p.Ser1064Gly
NM_001079817.1:c.3154A>G	NP_001073285.1:p.Ser1052Gly
NM_001079817.2:c.3154A>G	NP_001073285.1:p.Ser1052Gly
XM_011527988.1:c.3265A>G	XP_011526290.1:p.Ser1089Gly
XM_011527989.1:c.3229A>G	XP_011526291.1:p.Ser1077Gly
XM_011527988.2:c.3187A>G	XP_011526290.2:p.Ser1063Gly
XM_011527989.3:c.3151A>G	XP_011526291.2:p.Ser1051Gly
NM_000208.4:c.3190A>G MANE Select	NP_000199.2:p.Ser1064Gly
NM_001079817.3:c.3154A>G	NP_001073285.1:p.Ser1052Gly