Canonical Allele Identifier: CA403672008

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7132219G>C (hg19) ; chr19:g.7132208G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132208G>C , CM000681.2:g.7132208G>C	GRCh38
NC_000019.9:g.7132219G>C , CM000681.1:g.7132219G>C	GRCh37
NC_000019.8:g.7083219G>C	NCBI36
NG_008852.2:g.166793C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2792C>G MANE Select	ENSP00000303830.4:p.Ala931Gly
ENST00000302850.9:c.2792C>G	ENSP00000303830.4:p.Ala931Gly
ENST00000341500.9:c.2756C>G	ENSP00000342838.4:p.Ala919Gly
NM_000208.2:c.2792C>G	NP_000199.2:p.Ala931Gly
NM_000208.3:c.2792C>G	NP_000199.2:p.Ala931Gly
NM_001079817.1:c.2756C>G	NP_001073285.1:p.Ala919Gly
NM_001079817.2:c.2756C>G	NP_001073285.1:p.Ala919Gly
XM_011527988.1:c.2870C>G	XP_011526290.1:p.Ala957Gly
XM_011527989.1:c.2834C>G	XP_011526291.1:p.Ala945Gly
XM_011527988.2:c.2792C>G	XP_011526290.2:p.Ala931Gly
XM_011527989.3:c.2756C>G	XP_011526291.2:p.Ala919Gly
NM_000208.4:c.2792C>G MANE Select	NP_000199.2:p.Ala931Gly
NM_001079817.3:c.2756C>G	NP_001073285.1:p.Ala919Gly