Canonical Allele Identifier: CA403672134

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7132283C>G (hg19) ; chr19:g.7132272C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132272C>G , CM000681.2:g.7132272C>G	GRCh38
NC_000019.9:g.7132283C>G , CM000681.1:g.7132283C>G	GRCh37
NC_000019.8:g.7083283C>G	NCBI36
NG_008852.2:g.166729G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2728G>C MANE Select	ENSP00000303830.4:p.Gly910Arg
ENST00000302850.9:c.2728G>C	ENSP00000303830.4:p.Gly910Arg
ENST00000341500.9:c.2692G>C	ENSP00000342838.4:p.Gly898Arg
NM_000208.2:c.2728G>C	NP_000199.2:p.Gly910Arg
NM_000208.3:c.2728G>C	NP_000199.2:p.Gly910Arg
NM_001079817.1:c.2692G>C	NP_001073285.1:p.Gly898Arg
NM_001079817.2:c.2692G>C	NP_001073285.1:p.Gly898Arg
XM_011527988.1:c.2806G>C	XP_011526290.1:p.Gly936Arg
XM_011527989.1:c.2770G>C	XP_011526291.1:p.Gly924Arg
XM_011527988.2:c.2728G>C	XP_011526290.2:p.Gly910Arg
XM_011527989.3:c.2692G>C	XP_011526291.2:p.Gly898Arg
NM_000208.4:c.2728G>C MANE Select	NP_000199.2:p.Gly910Arg
NM_001079817.3:c.2692G>C	NP_001073285.1:p.Gly898Arg