Canonical Allele Identifier: CA403661884

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7141764G>C , CM000681.2:g.7141764G>C	GRCh38
NC_000019.9:g.7141775G>C , CM000681.1:g.7141775G>C	GRCh37
NC_000019.8:g.7092775G>C	NCBI36
NG_008852.2:g.157237C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000208.4:c.2595C>G MANE Select	NP_000199.2:p.Asn865Lys
ENST00000302850.10:c.2595C>G MANE Select	ENSP00000303830.4:p.Asn865Lys
NM_000208.2:c.2595C>G	NP_000199.2:p.Asn865Lys
NM_000208.3:c.2595C>G	NP_000199.2:p.Asn865Lys
NM_001079817.1:c.2559C>G	NP_001073285.1:p.Asn853Lys
NM_001079817.2:c.2559C>G	NP_001073285.1:p.Asn853Lys
NM_001079817.3:c.2559C>G	NP_001073285.1:p.Asn853Lys
ENST00000302850.9:c.2595C>G	ENSP00000303830.4:p.Asn865Lys
ENST00000341500.9:c.2559C>G	ENSP00000342838.4:p.Asn853Lys
ENST00000597211.1:n.278C>G
XM_011527988.1:c.2673C>G	XP_011526290.1:p.Asn891Lys
XM_011527988.2:c.2595C>G	XP_011526290.2:p.Asn865Lys
XM_011527989.1:c.2637C>G	XP_011526291.1:p.Asn879Lys
XM_011527989.3:c.2559C>G	XP_011526291.2:p.Asn853Lys