Canonical Allele Identifier: CA403671148

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125379G>C (hg19) ; chr19:g.7125368G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125368G>C , CM000681.2:g.7125368G>C	GRCh38
NC_000019.9:g.7125379G>C , CM000681.1:g.7125379G>C	GRCh37
NC_000019.8:g.7076379G>C	NCBI36
NG_008852.2:g.173633C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3173C>G MANE Select	ENSP00000303830.4:p.Thr1058Arg
ENST00000302850.9:c.3173C>G	ENSP00000303830.4:p.Thr1058Arg
ENST00000341500.9:c.3137C>G	ENSP00000342838.4:p.Thr1046Arg
ENST00000593970.1:n.19C>G
NM_000208.2:c.3173C>G	NP_000199.2:p.Thr1058Arg
NM_000208.3:c.3173C>G	NP_000199.2:p.Thr1058Arg
NM_001079817.1:c.3137C>G	NP_001073285.1:p.Thr1046Arg
NM_001079817.2:c.3137C>G	NP_001073285.1:p.Thr1046Arg
XM_011527988.1:c.3248C>G	XP_011526290.1:p.Thr1083Arg
XM_011527989.1:c.3212C>G	XP_011526291.1:p.Thr1071Arg
XM_011527988.2:c.3170C>G	XP_011526290.2:p.Thr1057Arg
XM_011527989.3:c.3134C>G	XP_011526291.2:p.Thr1045Arg
NM_000208.4:c.3173C>G MANE Select	NP_000199.2:p.Thr1058Arg
NM_001079817.3:c.3137C>G	NP_001073285.1:p.Thr1046Arg