Canonical Allele Identifier: CA505400208

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125375G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125364G>C , CM000681.2:g.7125364G>C	GRCh38
NC_000019.9:g.7125375G>C , CM000681.1:g.7125375G>C	GRCh37
NC_000019.8:g.7076375G>C	NCBI36
NG_008852.2:g.173637C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3177C>G MANE Select	ENSP00000303830.4:p.Val1059=
ENST00000302850.9:c.3177C>G	ENSP00000303830.4:p.Val1059=
ENST00000341500.9:c.3141C>G	ENSP00000342838.4:p.Val1047=
ENST00000593970.1:n.23C>G
NM_000208.2:c.3177C>G	NP_000199.2:p.Val1059=
NM_000208.3:c.3177C>G	NP_000199.2:p.Val1059=
NM_001079817.1:c.3141C>G	NP_001073285.1:p.Val1047=
NM_001079817.2:c.3141C>G	NP_001073285.1:p.Val1047=
XM_011527988.1:c.3252C>G	XP_011526290.1:p.Val1084=
XM_011527989.1:c.3216C>G	XP_011526291.1:p.Val1072=
XM_011527988.2:c.3174C>G	XP_011526290.2:p.Val1058=
XM_011527989.3:c.3138C>G	XP_011526291.2:p.Val1046=
NM_000208.4:c.3177C>G MANE Select	NP_000199.2:p.Val1059=
NM_001079817.3:c.3141C>G	NP_001073285.1:p.Val1047=