Canonical Allele Identifier: CA505204402

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7172374G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7172363G>T , CM000681.2:g.7172363G>T	GRCh38
NC_000019.9:g.7172374G>T , CM000681.1:g.7172374G>T	GRCh37
NC_000019.8:g.7123374G>T	NCBI36
NG_008852.2:g.126638C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1195C>A MANE Select	ENSP00000303830.4:p.Arg399=
ENST00000302850.9:c.1195C>A	ENSP00000303830.4:p.Arg399=
ENST00000341500.9:c.1195C>A	ENSP00000342838.4:p.Arg399=
ENST00000598216.1:n.1170C>A
NM_000208.2:c.1195C>A	NP_000199.2:p.Arg399=
NM_000208.3:c.1195C>A	NP_000199.2:p.Arg399=
NM_001079817.1:c.1195C>A	NP_001073285.1:p.Arg399=
NM_001079817.2:c.1195C>A	NP_001073285.1:p.Arg399=
XM_011527988.1:c.1273C>A	XP_011526290.1:p.Arg425=
XM_011527989.1:c.1273C>A	XP_011526291.1:p.Arg425=
XM_011527988.2:c.1195C>A	XP_011526290.2:p.Arg399=
XM_011527989.3:c.1195C>A	XP_011526291.2:p.Arg399=
NM_000208.4:c.1195C>A MANE Select	NP_000199.2:p.Arg399=
NM_001079817.3:c.1195C>A	NP_001073285.1:p.Arg399=