Canonical Allele Identifier: CA657054481

Gene: INSR

Linked Data

• dbSNP Id: rs1385343342
• COSMIC: COSN25750519
• MyVariant Identifiers: chr19:g.7129003G>A (hg19) ; chr19:g.7128992G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128992G>A , CM000681.2:g.7128992G>A	GRCh38
NC_000019.9:g.7129003G>A , CM000681.1:g.7129003G>A	GRCh37
NC_000019.8:g.7080003G>A	NCBI36
NG_008852.2:g.170009C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2843-38C>T MANE Select	ENSP00000303830.4:n.2843-38C>T
ENST00000302850.9:c.2843-38C>T	ENSP00000303830.4:n.2843-38C>T
ENST00000341500.9:c.2807-38C>T	ENSP00000342838.4:n.2807-38C>T
NM_000208.2:c.2843-38C>T	NP_000199.2:n.2843-38C>T
NM_000208.3:c.2843-38C>T	NP_000199.2:n.2843-38C>T
NM_001079817.1:c.2807-38C>T	NP_001073285.1:n.2807-38C>T
NM_001079817.2:c.2807-38C>T	NP_001073285.1:n.2807-38C>T
XM_011527988.1:c.2921-41C>T	XP_011526290.1:n.2921-41C>T
XM_011527989.1:c.2885-41C>T	XP_011526291.1:n.2885-41C>T
XM_011527988.2:c.2843-41C>T	XP_011526290.2:n.2843-41C>T
XM_011527989.3:c.2807-41C>T	XP_011526291.2:n.2807-41C>T
NM_000208.4:c.2843-38C>T MANE Select	NP_000199.2:n.2843-38C>T
NM_001079817.3:c.2807-38C>T	NP_001073285.1:n.2807-38C>T