Canonical Allele Identifier: CA403661620

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7141705G>C (hg19) ; chr19:g.7141694G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7141694G>C , CM000681.2:g.7141694G>C	GRCh38
NC_000019.9:g.7141705G>C , CM000681.1:g.7141705G>C	GRCh37
NC_000019.8:g.7092705G>C	NCBI36
NG_008852.2:g.157307C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2665C>G MANE Select	ENSP00000303830.4:p.Arg889Gly
ENST00000302850.9:c.2665C>G	ENSP00000303830.4:p.Arg889Gly
ENST00000341500.9:c.2629C>G	ENSP00000342838.4:p.Arg877Gly
ENST00000597211.1:n.348C>G
NM_000208.2:c.2665C>G	NP_000199.2:p.Arg889Gly
NM_000208.3:c.2665C>G	NP_000199.2:p.Arg889Gly
NM_001079817.1:c.2629C>G	NP_001073285.1:p.Arg877Gly
NM_001079817.2:c.2629C>G	NP_001073285.1:p.Arg877Gly
XM_011527988.1:c.2743C>G	XP_011526290.1:p.Arg915Gly
XM_011527989.1:c.2707C>G	XP_011526291.1:p.Arg903Gly
XM_011527988.2:c.2665C>G	XP_011526290.2:p.Arg889Gly
XM_011527989.3:c.2629C>G	XP_011526291.2:p.Arg877Gly
NM_000208.4:c.2665C>G MANE Select	NP_000199.2:p.Arg889Gly
NM_001079817.3:c.2629C>G	NP_001073285.1:p.Arg877Gly