Canonical Allele Identifier: CA505400068

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117229C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117218C>G , CM000681.2:g.7117218C>G	GRCh38
NC_000019.9:g.7117229C>G , CM000681.1:g.7117229C>G	GRCh37
NC_000019.8:g.7068229C>G	NCBI36
NG_008852.2:g.181783G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3987G>C MANE Select	ENSP00000303830.4:p.Leu1329=
ENST00000302850.9:c.3987G>C	ENSP00000303830.4:p.Leu1329=
ENST00000341500.9:c.3951G>C	ENSP00000342838.4:p.Leu1317=
NM_000208.2:c.3987G>C	NP_000199.2:p.Leu1329=
NM_000208.3:c.3987G>C	NP_000199.2:p.Leu1329=
NM_001079817.1:c.3951G>C	NP_001073285.1:p.Leu1317=
NM_001079817.2:c.3951G>C	NP_001073285.1:p.Leu1317=
XM_011527988.1:c.4062G>C	XP_011526290.1:p.Leu1354=
XM_011527989.1:c.4026G>C	XP_011526291.1:p.Leu1342=
XM_011527988.2:c.3984G>C	XP_011526290.2:p.Leu1328=
XM_011527989.3:c.3948G>C	XP_011526291.2:p.Leu1316=
NM_000208.4:c.3987G>C MANE Select	NP_000199.2:p.Leu1329=
NM_001079817.3:c.3951G>C	NP_001073285.1:p.Leu1317=