Canonical Allele Identifier: CA1355976956

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997240_32997242delinsTGG , CM000665.2:g.32997240_32997242delinsTGG	GRCh38
NC_000003.11:g.33038732_33038734delinsTGG , CM000665.1:g.33038732_33038734delinsTGG	GRCh37
NC_000003.10:g.33013736_33013738delinsTGG	NCBI36
NG_009005.1:g.104961_104963delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1837_1839delinsCCA MANE Select	ENSP00000306920.4:p.Pro613=
ENST00000307363.9:c.1837_1839delinsCCA	ENSP00000306920.4:p.Pro613=
ENST00000307377.12:c.1444_1446delinsCCA	ENSP00000305920.8:p.Pro482=
ENST00000399402.7:c.1747_1749delinsCCA	ENSP00000382333.2:p.Pro583=
NM_000404.2:c.1837_1839delinsCCA	NP_000395.2:p.Pro613=
NM_000404.3:c.1837_1839delinsCCA	NP_000395.2:p.Pro613=
NM_001079811.1:c.1747_1749delinsCCA	NP_001073279.1:p.Pro583=
NM_001079811.2:c.1747_1749delinsCCA	NP_001073279.1:p.Pro583=
NM_001135602.1:c.1444_1446delinsCCA	NP_001129074.1:p.Pro482=
NM_001135602.2:c.1444_1446delinsCCA	NP_001129074.1:p.Pro482=
NM_001317040.1:c.1981_1983delinsCCA	NP_001303969.1:p.Pro661=
NM_000404.4:c.1837_1839delinsCCA MANE Select	NP_000395.3:p.Pro613=
NM_001079811.3:c.1747_1749delinsCCA	NP_001073279.2:p.Pro583=
NM_001135602.3:c.1444_1446delinsCCA	NP_001129074.2:p.Pro482=
NM_001317040.2:c.1981_1983delinsCCA	NP_001303969.2:p.Pro661=
NM_001393580.1:c.1734+16814_1734+16816delinsCCA	NP_001380509.1:n.1734+16814_1734+16816delinsCCA