Canonical Allele Identifier: CA403668681

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117290T>G (hg19) ; chr19:g.7117279T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117279T>G , CM000681.2:g.7117279T>G	GRCh38
NC_000019.9:g.7117290T>G , CM000681.1:g.7117290T>G	GRCh37
NC_000019.8:g.7068290T>G	NCBI36
NG_008852.2:g.181722A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3926A>C MANE Select	ENSP00000303830.4:p.Asn1309Thr
ENST00000302850.9:c.3926A>C	ENSP00000303830.4:p.Asn1309Thr
ENST00000341500.9:c.3890A>C	ENSP00000342838.4:p.Asn1297Thr
NM_000208.2:c.3926A>C	NP_000199.2:p.Asn1309Thr
NM_000208.3:c.3926A>C	NP_000199.2:p.Asn1309Thr
NM_001079817.1:c.3890A>C	NP_001073285.1:p.Asn1297Thr
NM_001079817.2:c.3890A>C	NP_001073285.1:p.Asn1297Thr
XM_011527988.1:c.4001A>C	XP_011526290.1:p.Asn1334Thr
XM_011527989.1:c.3965A>C	XP_011526291.1:p.Asn1322Thr
XM_011527988.2:c.3923A>C	XP_011526290.2:p.Asn1308Thr
XM_011527989.3:c.3887A>C	XP_011526291.2:p.Asn1296Thr
NM_000208.4:c.3926A>C MANE Select	NP_000199.2:p.Asn1309Thr
NM_001079817.3:c.3890A>C	NP_001073285.1:p.Asn1297Thr