Canonical Allele Identifier: CA403671041

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125328G>C (hg19) ; chr19:g.7125317G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125317G>C , CM000681.2:g.7125317G>C	GRCh38
NC_000019.9:g.7125328G>C , CM000681.1:g.7125328G>C	GRCh37
NC_000019.8:g.7076328G>C	NCBI36
NG_008852.2:g.173684C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3224C>G MANE Select	ENSP00000303830.4:p.Ala1075Gly
ENST00000302850.9:c.3224C>G	ENSP00000303830.4:p.Ala1075Gly
ENST00000341500.9:c.3188C>G	ENSP00000342838.4:p.Ala1063Gly
ENST00000593970.1:n.70C>G
NM_000208.2:c.3224C>G	NP_000199.2:p.Ala1075Gly
NM_000208.3:c.3224C>G	NP_000199.2:p.Ala1075Gly
NM_001079817.1:c.3188C>G	NP_001073285.1:p.Ala1063Gly
NM_001079817.2:c.3188C>G	NP_001073285.1:p.Ala1063Gly
XM_011527988.1:c.3299C>G	XP_011526290.1:p.Ala1100Gly
XM_011527989.1:c.3263C>G	XP_011526291.1:p.Ala1088Gly
XM_011527988.2:c.3221C>G	XP_011526290.2:p.Ala1074Gly
XM_011527989.3:c.3185C>G	XP_011526291.2:p.Ala1062Gly
NM_000208.4:c.3224C>G MANE Select	NP_000199.2:p.Ala1075Gly
NM_001079817.3:c.3188C>G	NP_001073285.1:p.Ala1063Gly