Canonical Allele Identifier: CA1883798902

Gene: GLT6D1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135637909G= , CM000671.2:g.135637909G=	GRCh38
NC_000009.11:g.138529755G= , CM000671.1:g.138529755G=	GRCh37
NC_000009.10:g.137669576G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371763.6:c.71+1208C= MANE Select	ENSP00000360829.1:n.71+1208C=
ENST00000371763.5:c.71+1208C=	ENSP00000360829.1:n.71+1208C=
ENST00000613244.1:c.71+1208C=	ENSP00000483037.1:n.71+1208C=
NM_182974.2:c.71+1208C=	NP_892019.2:n.71+1208C=
XM_011518633.1:c.71+1208C=	XP_011516935.1:n.71+1208C=
XM_011518634.1:c.71+1208C=	XP_011516936.1:n.71+1208C=
XM_011518635.1:c.71+1208C=	XP_011516937.1:n.71+1208C=
XM_011518636.1:c.71+1208C=	XP_011516938.1:n.71+1208C=
XM_011518637.1:c.71+1208C=	XP_011516939.1:n.71+1208C=
XM_011518633.2:c.71+1208C=	XP_011516935.1:n.71+1208C=
XM_011518634.2:c.71+1208C=	XP_011516936.1:n.71+1208C=
XM_011518635.2:c.71+1208C=	XP_011516937.1:n.71+1208C=
XM_011518636.2:c.71+1208C=	XP_011516938.1:n.71+1208C=
XM_011518637.2:c.71+1208C=	XP_011516939.1:n.71+1208C=
XM_024447534.1:c.71+1208C=	XP_024303302.1:n.71+1208C=
NM_182974.3:c.71+1208C= MANE Select	NP_892019.2:n.71+1208C=