Canonical Allele Identifier: CA505216637

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7120654G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120643G>C , CM000681.2:g.7120643G>C	GRCh38
NC_000019.9:g.7120654G>C , CM000681.1:g.7120654G>C	GRCh37
NC_000019.8:g.7071654G>C	NCBI36
NG_008852.2:g.178358C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3636C>G MANE Select	ENSP00000303830.4:p.Val1212=
ENST00000302850.9:c.3636C>G	ENSP00000303830.4:p.Val1212=
ENST00000341500.9:c.3600C>G	ENSP00000342838.4:p.Val1200=
ENST00000601099.1:n.547C>G
NM_000208.2:c.3636C>G	NP_000199.2:p.Val1212=
NM_000208.3:c.3636C>G	NP_000199.2:p.Val1212=
NM_001079817.1:c.3600C>G	NP_001073285.1:p.Val1200=
NM_001079817.2:c.3600C>G	NP_001073285.1:p.Val1200=
XM_011527988.1:c.3711C>G	XP_011526290.1:p.Val1237=
XM_011527989.1:c.3675C>G	XP_011526291.1:p.Val1225=
XM_011527988.2:c.3633C>G	XP_011526290.2:p.Val1211=
XM_011527989.3:c.3597C>G	XP_011526291.2:p.Val1199=
NM_000208.4:c.3636C>G MANE Select	NP_000199.2:p.Val1212=
NM_001079817.3:c.3600C>G	NP_001073285.1:p.Val1200=