Canonical Allele Identifier: CA2587921670

Gene: INSR

Linked Data

• gnomAD v4: 19-7122838-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122838G>A , CM000681.2:g.7122838G>A	GRCh38
NC_000019.9:g.7122849G>A , CM000681.1:g.7122849G>A	GRCh37
NC_000019.8:g.7073849G>A	NCBI36
NG_008852.2:g.176163C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3369+41C>T MANE Select	ENSP00000303830.4:n.3369+41C>T
ENST00000302850.9:c.3369+41C>T	ENSP00000303830.4:n.3369+41C>T
ENST00000341500.9:c.3333+41C>T	ENSP00000342838.4:n.3333+41C>T
ENST00000593970.1:n.215+41C>T
ENST00000601099.1:n.280+41C>T
NM_000208.2:c.3369+41C>T	NP_000199.2:n.3369+41C>T
NM_000208.3:c.3369+41C>T	NP_000199.2:n.3369+41C>T
NM_001079817.1:c.3333+41C>T	NP_001073285.1:n.3333+41C>T
NM_001079817.2:c.3333+41C>T	NP_001073285.1:n.3333+41C>T
XM_011527988.1:c.3444+41C>T	XP_011526290.1:n.3444+41C>T
XM_011527989.1:c.3408+41C>T	XP_011526291.1:n.3408+41C>T
XM_011527988.2:c.3366+41C>T	XP_011526290.2:n.3366+41C>T
XM_011527989.3:c.3330+41C>T	XP_011526291.2:n.3330+41C>T
NM_000208.4:c.3369+41C>T MANE Select	NP_000199.2:n.3369+41C>T
NM_001079817.3:c.3333+41C>T	NP_001073285.1:n.3333+41C>T