Canonical Allele Identifier: CA9136077

Gene: INSR

Linked Data

• dbSNP Id: rs766415072
• ExAC: 19:7184684 A / G
• gnomAD v2: 19-7184684-A-G
• gnomAD v3: 19-7184673-A-G
• gnomAD v4: 19-7184673-A-G
• MyVariant Identifiers: chr19:g.7184684A>G (hg19) ; chr19:g.7184673A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184673A>G , CM000681.2:g.7184673A>G	GRCh38
NC_000019.9:g.7184684A>G , CM000681.1:g.7184684A>G	GRCh37
NC_000019.8:g.7135684A>G	NCBI36
NG_008852.2:g.114328T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-36T>C MANE Select	ENSP00000303830.4:n.653-36T>C
ENST00000302850.9:c.653-36T>C	ENSP00000303830.4:n.653-36T>C
ENST00000341500.9:c.653-36T>C	ENSP00000342838.4:n.653-36T>C
ENST00000598216.1:n.628-36T>C
NM_000208.2:c.653-36T>C	NP_000199.2:n.653-36T>C
NM_000208.3:c.653-36T>C	NP_000199.2:n.653-36T>C
NM_001079817.1:c.653-36T>C	NP_001073285.1:n.653-36T>C
NM_001079817.2:c.653-36T>C	NP_001073285.1:n.653-36T>C
XM_011527988.1:c.731-36T>C	XP_011526290.1:n.731-36T>C
XM_011527989.1:c.731-36T>C	XP_011526291.1:n.731-36T>C
XM_011527988.2:c.653-36T>C	XP_011526290.2:n.653-36T>C
XM_011527989.3:c.653-36T>C	XP_011526291.2:n.653-36T>C
NM_000208.4:c.653-36T>C MANE Select	NP_000199.2:n.653-36T>C
NM_001079817.3:c.653-36T>C	NP_001073285.1:n.653-36T>C