Canonical Allele Identifier: CA403671924

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7132182G>C (hg19) ; chr19:g.7132171G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132171G>C , CM000681.2:g.7132171G>C	GRCh38
NC_000019.9:g.7132182G>C , CM000681.1:g.7132182G>C	GRCh37
NC_000019.8:g.7083182G>C	NCBI36
NG_008852.2:g.166830C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2829C>G MANE Select	ENSP00000303830.4:p.Tyr943Ter
ENST00000302850.9:c.2829C>G	ENSP00000303830.4:p.Tyr943Ter
ENST00000341500.9:c.2793C>G	ENSP00000342838.4:p.Tyr931Ter
NM_000208.2:c.2829C>G	NP_000199.2:p.Tyr943Ter
NM_000208.3:c.2829C>G	NP_000199.2:p.Tyr943Ter
NM_001079817.1:c.2793C>G	NP_001073285.1:p.Tyr931Ter
NM_001079817.2:c.2793C>G	NP_001073285.1:p.Tyr931Ter
XM_011527988.1:c.2907C>G	XP_011526290.1:p.Tyr969Ter
XM_011527989.1:c.2871C>G	XP_011526291.1:p.Tyr957Ter
XM_011527988.2:c.2829C>G	XP_011526290.2:p.Tyr943Ter
XM_011527989.3:c.2793C>G	XP_011526291.2:p.Tyr931Ter
NM_000208.4:c.2829C>G MANE Select	NP_000199.2:p.Tyr943Ter
NM_001079817.3:c.2793C>G	NP_001073285.1:p.Tyr931Ter