Canonical Allele Identifier: CA403669440

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7120688C>G (hg19) ; chr19:g.7120677C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120677C>G , CM000681.2:g.7120677C>G	GRCh38
NC_000019.9:g.7120688C>G , CM000681.1:g.7120688C>G	GRCh37
NC_000019.8:g.7071688C>G	NCBI36
NG_008852.2:g.178324G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3602G>C MANE Select	ENSP00000303830.4:p.Arg1201Pro
ENST00000302850.9:c.3602G>C	ENSP00000303830.4:p.Arg1201Pro
ENST00000341500.9:c.3566G>C	ENSP00000342838.4:p.Arg1189Pro
ENST00000601099.1:n.513G>C
NM_000208.2:c.3602G>C	NP_000199.2:p.Arg1201Pro
NM_000208.3:c.3602G>C	NP_000199.2:p.Arg1201Pro
NM_001079817.1:c.3566G>C	NP_001073285.1:p.Arg1189Pro
NM_001079817.2:c.3566G>C	NP_001073285.1:p.Arg1189Pro
XM_011527988.1:c.3677G>C	XP_011526290.1:p.Arg1226Pro
XM_011527989.1:c.3641G>C	XP_011526291.1:p.Arg1214Pro
XM_011527988.2:c.3599G>C	XP_011526290.2:p.Arg1200Pro
XM_011527989.3:c.3563G>C	XP_011526291.2:p.Arg1188Pro
NM_000208.4:c.3602G>C MANE Select	NP_000199.2:p.Arg1201Pro
NM_001079817.3:c.3566G>C	NP_001073285.1:p.Arg1189Pro