Canonical Allele Identifier: CA2695228017

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125279T>C , CM000681.2:g.7125279T>C	GRCh38
NC_000019.9:g.7125290T>C , CM000681.1:g.7125290T>C	GRCh37
NC_000019.8:g.7076290T>C	NCBI36
NG_008852.2:g.173722A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3258+4A>G MANE Select	ENSP00000303830.4:n.3258+4A>G
ENST00000302850.9:c.3258+4A>G	ENSP00000303830.4:n.3258+4A>G
ENST00000341500.9:c.3222+4A>G	ENSP00000342838.4:n.3222+4A>G
ENST00000593970.1:n.104+4A>G
NM_000208.2:c.3258+4A>G	NP_000199.2:n.3258+4A>G
NM_000208.3:c.3258+4A>G	NP_000199.2:n.3258+4A>G
NM_001079817.1:c.3222+4A>G	NP_001073285.1:n.3222+4A>G
NM_001079817.2:c.3222+4A>G	NP_001073285.1:n.3222+4A>G
XM_011527988.1:c.3333+4A>G	XP_011526290.1:n.3333+4A>G
XM_011527989.1:c.3297+4A>G	XP_011526291.1:n.3297+4A>G
XM_011527988.2:c.3255+4A>G	XP_011526290.2:n.3255+4A>G
XM_011527989.3:c.3219+4A>G	XP_011526291.2:n.3219+4A>G
NM_000208.4:c.3258+4A>G MANE Select	NP_000199.2:n.3258+4A>G
NM_001079817.3:c.3222+4A>G	NP_001073285.1:n.3222+4A>G