Canonical Allele Identifier: CA403667264

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7170645G>C (hg19) ; chr19:g.7170634G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7170634G>C , CM000681.2:g.7170634G>C	GRCh38
NC_000019.9:g.7170645G>C , CM000681.1:g.7170645G>C	GRCh37
NC_000019.8:g.7121645G>C	NCBI36
NG_008852.2:g.128367C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1386C>G MANE Select	ENSP00000303830.4:p.Cys462Trp
ENST00000302850.9:c.1386C>G	ENSP00000303830.4:p.Cys462Trp
ENST00000341500.9:c.1386C>G	ENSP00000342838.4:p.Cys462Trp
ENST00000598216.1:n.1361C>G
NM_000208.2:c.1386C>G	NP_000199.2:p.Cys462Trp
NM_000208.3:c.1386C>G	NP_000199.2:p.Cys462Trp
NM_001079817.1:c.1386C>G	NP_001073285.1:p.Cys462Trp
NM_001079817.2:c.1386C>G	NP_001073285.1:p.Cys462Trp
XM_011527988.1:c.1464C>G	XP_011526290.1:p.Cys488Trp
XM_011527989.1:c.1464C>G	XP_011526291.1:p.Cys488Trp
XM_011527988.2:c.1386C>G	XP_011526290.2:p.Cys462Trp
XM_011527989.3:c.1386C>G	XP_011526291.2:p.Cys462Trp
NM_000208.4:c.1386C>G MANE Select	NP_000199.2:p.Cys462Trp
NM_001079817.3:c.1386C>G	NP_001073285.1:p.Cys462Trp