Canonical Allele Identifier: CA304856298

Gene: INSR

Linked Data

• dbSNP Id: rs921044638
• MyVariant Identifiers: chr19:g.7166382C>T (hg19) ; chr19:g.7166371C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166371C>T , CM000681.2:g.7166371C>T	GRCh38
NC_000019.9:g.7166382C>T , CM000681.1:g.7166382C>T	GRCh37
NC_000019.8:g.7117382C>T	NCBI36
NG_008852.2:g.132630G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.1644G>A MANE Select	ENSP00000303830.4:p.Gln548=
ENST00000302850.9:c.1644G>A	ENSP00000303830.4:p.Gln548=
ENST00000341500.9:c.1644G>A	ENSP00000342838.4:p.Gln548=
ENST00000598216.1:n.1619G>A
ENST00000600492.1:c.45G>A	ENSP00000473170.1:p.Gln15=
NM_000208.2:c.1644G>A	NP_000199.2:p.Gln548=
NM_000208.3:c.1644G>A	NP_000199.2:p.Gln548=
NM_001079817.1:c.1644G>A	NP_001073285.1:p.Gln548=
NM_001079817.2:c.1644G>A	NP_001073285.1:p.Gln548=
XM_011527988.1:c.1722G>A	XP_011526290.1:p.Gln574=
XM_011527989.1:c.1722G>A	XP_011526291.1:p.Gln574=
XM_011527988.2:c.1644G>A	XP_011526290.2:p.Gln548=
XM_011527989.3:c.1644G>A	XP_011526291.2:p.Gln548=
NM_000208.4:c.1644G>A MANE Select	NP_000199.2:p.Gln548=
NM_001079817.3:c.1644G>A	NP_001073285.1:p.Gln548=