Canonical Allele Identifier: CA505400259

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125462C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125451C>G , CM000681.2:g.7125451C>G	GRCh38
NC_000019.9:g.7125462C>G , CM000681.1:g.7125462C>G	GRCh37
NC_000019.8:g.7076462C>G	NCBI36
NG_008852.2:g.173550G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3090G>C MANE Select	ENSP00000303830.4:p.Gly1030=
ENST00000302850.9:c.3090G>C	ENSP00000303830.4:p.Gly1030=
ENST00000341500.9:c.3054G>C	ENSP00000342838.4:p.Gly1018=
NM_000208.2:c.3090G>C	NP_000199.2:p.Gly1030=
NM_000208.3:c.3090G>C	NP_000199.2:p.Gly1030=
NM_001079817.1:c.3054G>C	NP_001073285.1:p.Gly1018=
NM_001079817.2:c.3054G>C	NP_001073285.1:p.Gly1018=
XM_011527988.1:c.3165G>C	XP_011526290.1:p.Gly1055=
XM_011527989.1:c.3129G>C	XP_011526291.1:p.Gly1043=
XM_011527988.2:c.3087G>C	XP_011526290.2:p.Gly1029=
XM_011527989.3:c.3051G>C	XP_011526291.2:p.Gly1017=
NM_000208.4:c.3090G>C MANE Select	NP_000199.2:p.Gly1030=
NM_001079817.3:c.3054G>C	NP_001073285.1:p.Gly1018=