Canonical Allele Identifier: CA2320766507

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122940A= , CM000681.2:g.7122940A=	GRCh38
NC_000019.9:g.7122951A= , CM000681.1:g.7122951A=	GRCh37
NC_000019.8:g.7073951A=	NCBI36
NG_008852.2:g.176061T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3308T= MANE Select	ENSP00000303830.4:p.Met1103=
ENST00000302850.9:c.3308T=	ENSP00000303830.4:p.Met1103=
ENST00000341500.9:c.3272T=	ENSP00000342838.4:p.Met1091=
ENST00000593970.1:n.154T=
ENST00000601099.1:n.219T=
NM_000208.2:c.3308T=	NP_000199.2:p.Met1103=
NM_000208.3:c.3308T=	NP_000199.2:p.Met1103=
NM_001079817.1:c.3272T=	NP_001073285.1:p.Met1091=
NM_001079817.2:c.3272T=	NP_001073285.1:p.Met1091=
XM_011527988.1:c.3383T=	XP_011526290.1:p.Met1128=
XM_011527989.1:c.3347T=	XP_011526291.1:p.Met1116=
XM_011527988.2:c.3305T=	XP_011526290.2:p.Met1102=
XM_011527989.3:c.3269T=	XP_011526291.2:p.Met1090=
NM_000208.4:c.3308T= MANE Select	NP_000199.2:p.Met1103=
NM_001079817.3:c.3272T=	NP_001073285.1:p.Met1091=