Canonical Allele Identifier: CA403669922

Gene: INSR

Linked Data

• gnomAD v4: 19-7184445-T-G
• MyVariant Identifiers: chr19:g.7184456T>G (hg19) ; chr19:g.7184445T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184445T>G , CM000681.2:g.7184445T>G	GRCh38
NC_000019.9:g.7184456T>G , CM000681.1:g.7184456T>G	GRCh37
NC_000019.8:g.7135456T>G	NCBI36
NG_008852.2:g.114556A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.845A>C MANE Select	ENSP00000303830.4:p.Asn282Thr
ENST00000302850.9:c.845A>C	ENSP00000303830.4:p.Asn282Thr
ENST00000341500.9:c.845A>C	ENSP00000342838.4:p.Asn282Thr
ENST00000598216.1:n.820A>C
NM_000208.2:c.845A>C	NP_000199.2:p.Asn282Thr
NM_000208.3:c.845A>C	NP_000199.2:p.Asn282Thr
NM_001079817.1:c.845A>C	NP_001073285.1:p.Asn282Thr
NM_001079817.2:c.845A>C	NP_001073285.1:p.Asn282Thr
XM_011527988.1:c.923A>C	XP_011526290.1:p.Asn308Thr
XM_011527989.1:c.923A>C	XP_011526291.1:p.Asn308Thr
XM_011527988.2:c.845A>C	XP_011526290.2:p.Asn282Thr
XM_011527989.3:c.845A>C	XP_011526291.2:p.Asn282Thr
NM_000208.4:c.845A>C MANE Select	NP_000199.2:p.Asn282Thr
NM_001079817.3:c.845A>C	NP_001073285.1:p.Asn282Thr