Canonical Allele Identifier: CA403671118

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125364G>C (hg19) ; chr19:g.7125353G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125353G>C , CM000681.2:g.7125353G>C	GRCh38
NC_000019.9:g.7125364G>C , CM000681.1:g.7125364G>C	GRCh37
NC_000019.8:g.7076364G>C	NCBI36
NG_008852.2:g.173648C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3188C>G MANE Select	ENSP00000303830.4:p.Ala1063Gly
ENST00000302850.9:c.3188C>G	ENSP00000303830.4:p.Ala1063Gly
ENST00000341500.9:c.3152C>G	ENSP00000342838.4:p.Ala1051Gly
ENST00000593970.1:n.34C>G
NM_000208.2:c.3188C>G	NP_000199.2:p.Ala1063Gly
NM_000208.3:c.3188C>G	NP_000199.2:p.Ala1063Gly
NM_001079817.1:c.3152C>G	NP_001073285.1:p.Ala1051Gly
NM_001079817.2:c.3152C>G	NP_001073285.1:p.Ala1051Gly
XM_011527988.1:c.3263C>G	XP_011526290.1:p.Ala1088Gly
XM_011527989.1:c.3227C>G	XP_011526291.1:p.Ala1076Gly
XM_011527988.2:c.3185C>G	XP_011526290.2:p.Ala1062Gly
XM_011527989.3:c.3149C>G	XP_011526291.2:p.Ala1050Gly
NM_000208.4:c.3188C>G MANE Select	NP_000199.2:p.Ala1063Gly
NM_001079817.3:c.3152C>G	NP_001073285.1:p.Ala1051Gly