Canonical Allele Identifier: CA505216687

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7120699C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120688C>T , CM000681.2:g.7120688C>T	GRCh38
NC_000019.9:g.7120699C>T , CM000681.1:g.7120699C>T	GRCh37
NC_000019.8:g.7071699C>T	NCBI36
NG_008852.2:g.178313G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3591G>A MANE Select	ENSP00000303830.4:p.Leu1197=
ENST00000302850.9:c.3591G>A	ENSP00000303830.4:p.Leu1197=
ENST00000341500.9:c.3555G>A	ENSP00000342838.4:p.Leu1185=
ENST00000601099.1:n.502G>A
NM_000208.2:c.3591G>A	NP_000199.2:p.Leu1197=
NM_000208.3:c.3591G>A	NP_000199.2:p.Leu1197=
NM_001079817.1:c.3555G>A	NP_001073285.1:p.Leu1185=
NM_001079817.2:c.3555G>A	NP_001073285.1:p.Leu1185=
XM_011527988.1:c.3666G>A	XP_011526290.1:p.Leu1222=
XM_011527989.1:c.3630G>A	XP_011526291.1:p.Leu1210=
XM_011527988.2:c.3588G>A	XP_011526290.2:p.Leu1196=
XM_011527989.3:c.3552G>A	XP_011526291.2:p.Leu1184=
NM_000208.4:c.3591G>A MANE Select	NP_000199.2:p.Leu1197=
NM_001079817.3:c.3555G>A	NP_001073285.1:p.Leu1185=