Canonical Allele Identifier: CA505400341

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7184404C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184393C>T , CM000681.2:g.7184393C>T	GRCh38
NC_000019.9:g.7184404C>T , CM000681.1:g.7184404C>T	GRCh37
NC_000019.8:g.7135404C>T	NCBI36
NG_008852.2:g.114608G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.897G>A MANE Select	ENSP00000303830.4:p.Gln299=
ENST00000302850.9:c.897G>A	ENSP00000303830.4:p.Gln299=
ENST00000341500.9:c.897G>A	ENSP00000342838.4:p.Gln299=
ENST00000598216.1:n.872G>A
NM_000208.2:c.897G>A	NP_000199.2:p.Gln299=
NM_000208.3:c.897G>A	NP_000199.2:p.Gln299=
NM_001079817.1:c.897G>A	NP_001073285.1:p.Gln299=
NM_001079817.2:c.897G>A	NP_001073285.1:p.Gln299=
XM_011527988.1:c.975G>A	XP_011526290.1:p.Gln325=
XM_011527989.1:c.975G>A	XP_011526291.1:p.Gln325=
XM_011527988.2:c.897G>A	XP_011526290.2:p.Gln299=
XM_011527989.3:c.897G>A	XP_011526291.2:p.Gln299=
NM_000208.4:c.897G>A MANE Select	NP_000199.2:p.Gln299=
NM_001079817.3:c.897G>A	NP_001073285.1:p.Gln299=