Canonical Allele Identifier: CA2320796110

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184344G= , CM000681.2:g.7184344G=	GRCh38
NC_000019.9:g.7184355G= , CM000681.1:g.7184355G=	GRCh37
NC_000019.8:g.7135355G=	NCBI36
NG_008852.2:g.114657C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.946C= MANE Select	ENSP00000303830.4:p.Pro316=
ENST00000302850.9:c.946C=	ENSP00000303830.4:p.Pro316=
ENST00000341500.9:c.946C=	ENSP00000342838.4:p.Pro316=
ENST00000598216.1:n.921C=
NM_000208.2:c.946C=	NP_000199.2:p.Pro316=
NM_000208.3:c.946C=	NP_000199.2:p.Pro316=
NM_001079817.1:c.946C=	NP_001073285.1:p.Pro316=
NM_001079817.2:c.946C=	NP_001073285.1:p.Pro316=
XM_011527988.1:c.1024C=	XP_011526290.1:p.Pro342=
XM_011527989.1:c.1024C=	XP_011526291.1:p.Pro342=
XM_011527988.2:c.946C=	XP_011526290.2:p.Pro316=
XM_011527989.3:c.946C=	XP_011526291.2:p.Pro316=
NM_000208.4:c.946C= MANE Select	NP_000199.2:p.Pro316=
NM_001079817.3:c.946C=	NP_001073285.1:p.Pro316=