Canonical Allele Identifier: CA2320771118

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132336_7132339delinsGAGA , CM000681.2:g.7132336_7132339delinsGAGA	GRCh38
NC_000019.9:g.7132347_7132350delinsGAGA , CM000681.1:g.7132347_7132350delinsGAGA	GRCh37
NC_000019.8:g.7083347_7083350delinsGAGA	NCBI36
NG_008852.2:g.166662_166665delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2683-22_2683-19delinsTCTC MANE Select	ENSP00000303830.4:n.2683-22_2683-19delinsTCTC
ENST00000302850.9:c.2683-22_2683-19delinsTCTC	ENSP00000303830.4:n.2683-22_2683-19delinsTCTC
ENST00000341500.9:c.2647-22_2647-19delinsTCTC	ENSP00000342838.4:n.2647-22_2647-19delinsTCTC
NM_000208.2:c.2683-22_2683-19delinsTCTC	NP_000199.2:n.2683-22_2683-19delinsTCTC
NM_000208.3:c.2683-22_2683-19delinsTCTC	NP_000199.2:n.2683-22_2683-19delinsTCTC
NM_001079817.1:c.2647-22_2647-19delinsTCTC	NP_001073285.1:n.2647-22_2647-19delinsTCTC
NM_001079817.2:c.2647-22_2647-19delinsTCTC	NP_001073285.1:n.2647-22_2647-19delinsTCTC
XM_011527988.1:c.2761-22_2761-19delinsTCTC	XP_011526290.1:n.2761-22_2761-19delinsTCTC
XM_011527989.1:c.2725-22_2725-19delinsTCTC	XP_011526291.1:n.2725-22_2725-19delinsTCTC
XM_011527988.2:c.2683-22_2683-19delinsTCTC	XP_011526290.2:n.2683-22_2683-19delinsTCTC
XM_011527989.3:c.2647-22_2647-19delinsTCTC	XP_011526291.2:n.2647-22_2647-19delinsTCTC
NM_000208.4:c.2683-22_2683-19delinsTCTC MANE Select	NP_000199.2:n.2683-22_2683-19delinsTCTC
NM_001079817.3:c.2647-22_2647-19delinsTCTC	NP_001073285.1:n.2647-22_2647-19delinsTCTC