Canonical Allele Identifier: CA505400361

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7142978A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7142967A>G , CM000681.2:g.7142967A>G	GRCh38
NC_000019.9:g.7142978A>G , CM000681.1:g.7142978A>G	GRCh37
NC_000019.8:g.7093978A>G	NCBI36
NG_008852.2:g.156034T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2391T>C MANE Select	ENSP00000303830.4:p.Pro797=
ENST00000302850.9:c.2391T>C	ENSP00000303830.4:p.Pro797=
ENST00000341500.9:c.2355T>C	ENSP00000342838.4:p.Pro785=
ENST00000597211.1:n.74T>C
NM_000208.2:c.2391T>C	NP_000199.2:p.Pro797=
NM_000208.3:c.2391T>C	NP_000199.2:p.Pro797=
NM_001079817.1:c.2355T>C	NP_001073285.1:p.Pro785=
NM_001079817.2:c.2355T>C	NP_001073285.1:p.Pro785=
XM_011527988.1:c.2469T>C	XP_011526290.1:p.Pro823=
XM_011527989.1:c.2433T>C	XP_011526291.1:p.Pro811=
XM_011527988.2:c.2391T>C	XP_011526290.2:p.Pro797=
XM_011527989.3:c.2355T>C	XP_011526291.2:p.Pro785=
NM_000208.4:c.2391T>C MANE Select	NP_000199.2:p.Pro797=
NM_001079817.3:c.2355T>C	NP_001073285.1:p.Pro785=