Canonical Allele Identifier: CA505400175

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125321G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125310G>C , CM000681.2:g.7125310G>C	GRCh38
NC_000019.9:g.7125321G>C , CM000681.1:g.7125321G>C	GRCh37
NC_000019.8:g.7076321G>C	NCBI36
NG_008852.2:g.173691C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3231C>G MANE Select	ENSP00000303830.4:p.Val1077=
ENST00000302850.9:c.3231C>G	ENSP00000303830.4:p.Val1077=
ENST00000341500.9:c.3195C>G	ENSP00000342838.4:p.Val1065=
ENST00000593970.1:n.77C>G
NM_000208.2:c.3231C>G	NP_000199.2:p.Val1077=
NM_000208.3:c.3231C>G	NP_000199.2:p.Val1077=
NM_001079817.1:c.3195C>G	NP_001073285.1:p.Val1065=
NM_001079817.2:c.3195C>G	NP_001073285.1:p.Val1065=
XM_011527988.1:c.3306C>G	XP_011526290.1:p.Val1102=
XM_011527989.1:c.3270C>G	XP_011526291.1:p.Val1090=
XM_011527988.2:c.3228C>G	XP_011526290.2:p.Val1076=
XM_011527989.3:c.3192C>G	XP_011526291.2:p.Val1064=
NM_000208.4:c.3231C>G MANE Select	NP_000199.2:p.Val1077=
NM_001079817.3:c.3195C>G	NP_001073285.1:p.Val1065=