Canonical Allele Identifier: CA505217368

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128877T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128866T>C , CM000681.2:g.7128866T>C	GRCh38
NC_000019.9:g.7128877T>C , CM000681.1:g.7128877T>C	GRCh37
NC_000019.8:g.7079877T>C	NCBI36
NG_008852.2:g.170135A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2931A>G MANE Select	ENSP00000303830.4:p.Leu977=
ENST00000302850.9:c.2931A>G	ENSP00000303830.4:p.Leu977=
ENST00000341500.9:c.2895A>G	ENSP00000342838.4:p.Leu965=
NM_000208.2:c.2931A>G	NP_000199.2:p.Leu977=
NM_000208.3:c.2931A>G	NP_000199.2:p.Leu977=
NM_001079817.1:c.2895A>G	NP_001073285.1:p.Leu965=
NM_001079817.2:c.2895A>G	NP_001073285.1:p.Leu965=
XM_011527988.1:c.3006A>G	XP_011526290.1:p.Leu1002=
XM_011527989.1:c.2970A>G	XP_011526291.1:p.Leu990=
XM_011527988.2:c.2928A>G	XP_011526290.2:p.Leu976=
XM_011527989.3:c.2892A>G	XP_011526291.2:p.Leu964=
NM_000208.4:c.2931A>G MANE Select	NP_000199.2:p.Leu977=
NM_001079817.3:c.2895A>G	NP_001073285.1:p.Leu965=