Canonical Allele Identifier: CA505400438

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7143077A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7143066A>G , CM000681.2:g.7143066A>G	GRCh38
NC_000019.9:g.7143077A>G , CM000681.1:g.7143077A>G	GRCh37
NC_000019.8:g.7094077A>G	NCBI36
NG_008852.2:g.155935T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2292T>C MANE Select	ENSP00000303830.4:p.Leu764=
ENST00000302850.9:c.2292T>C	ENSP00000303830.4:p.Leu764=
ENST00000341500.9:c.2256T>C	ENSP00000342838.4:p.Leu752=
NM_000208.2:c.2292T>C	NP_000199.2:p.Leu764=
NM_000208.3:c.2292T>C	NP_000199.2:p.Leu764=
NM_001079817.1:c.2256T>C	NP_001073285.1:p.Leu752=
NM_001079817.2:c.2256T>C	NP_001073285.1:p.Leu752=
XM_011527988.1:c.2370T>C	XP_011526290.1:p.Leu790=
XM_011527989.1:c.2334T>C	XP_011526291.1:p.Leu778=
XM_011527988.2:c.2292T>C	XP_011526290.2:p.Leu764=
XM_011527989.3:c.2256T>C	XP_011526291.2:p.Leu752=
NM_000208.4:c.2292T>C MANE Select	NP_000199.2:p.Leu764=
NM_001079817.3:c.2256T>C	NP_001073285.1:p.Leu752=