Canonical Allele Identifier: CA2576594980

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122847A>C , CM000681.2:g.7122847A>C	GRCh38
NC_000019.9:g.7122858A>C , CM000681.1:g.7122858A>C	GRCh37
NC_000019.8:g.7073858A>C	NCBI36
NG_008852.2:g.176154T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3369+32T>G MANE Select	ENSP00000303830.4:n.3369+32T>G
ENST00000302850.9:c.3369+32T>G	ENSP00000303830.4:n.3369+32T>G
ENST00000341500.9:c.3333+32T>G	ENSP00000342838.4:n.3333+32T>G
ENST00000593970.1:n.215+32T>G
ENST00000601099.1:n.280+32T>G
NM_000208.2:c.3369+32T>G	NP_000199.2:n.3369+32T>G
NM_000208.3:c.3369+32T>G	NP_000199.2:n.3369+32T>G
NM_001079817.1:c.3333+32T>G	NP_001073285.1:n.3333+32T>G
NM_001079817.2:c.3333+32T>G	NP_001073285.1:n.3333+32T>G
XM_011527988.1:c.3444+32T>G	XP_011526290.1:n.3444+32T>G
XM_011527989.1:c.3408+32T>G	XP_011526291.1:n.3408+32T>G
XM_011527988.2:c.3366+32T>G	XP_011526290.2:n.3366+32T>G
XM_011527989.3:c.3330+32T>G	XP_011526291.2:n.3330+32T>G
NM_000208.4:c.3369+32T>G MANE Select	NP_000199.2:n.3369+32T>G
NM_001079817.3:c.3333+32T>G	NP_001073285.1:n.3333+32T>G