Canonical Allele Identifier: CA2587922508

Gene: INSR

Linked Data

• gnomAD v4: 19-7129040-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7129040G>T , CM000681.2:g.7129040G>T	GRCh38
NC_000019.9:g.7129051G>T , CM000681.1:g.7129051G>T	GRCh37
NC_000019.8:g.7080051G>T	NCBI36
NG_008852.2:g.169961C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2843-86C>A MANE Select	ENSP00000303830.4:n.2843-86C>A
ENST00000302850.9:c.2843-86C>A	ENSP00000303830.4:n.2843-86C>A
ENST00000341500.9:c.2807-86C>A	ENSP00000342838.4:n.2807-86C>A
NM_000208.2:c.2843-86C>A	NP_000199.2:n.2843-86C>A
NM_000208.3:c.2843-86C>A	NP_000199.2:n.2843-86C>A
NM_001079817.1:c.2807-86C>A	NP_001073285.1:n.2807-86C>A
NM_001079817.2:c.2807-86C>A	NP_001073285.1:n.2807-86C>A
XM_011527988.1:c.2921-89C>A	XP_011526290.1:n.2921-89C>A
XM_011527989.1:c.2885-89C>A	XP_011526291.1:n.2885-89C>A
XM_011527988.2:c.2843-89C>A	XP_011526290.2:n.2843-89C>A
XM_011527989.3:c.2807-89C>A	XP_011526291.2:n.2807-89C>A
NM_000208.4:c.2843-86C>A MANE Select	NP_000199.2:n.2843-86C>A
NM_001079817.3:c.2807-86C>A	NP_001073285.1:n.2807-86C>A