Canonical Allele Identifier: CA2407042042

Gene: TTLL1 TTLL1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43039726C= , CM000684.2:g.43039726C=	GRCh38
NC_000022.10:g.43435732C= , CM000684.1:g.43435732C=	GRCh37
NC_000022.9:g.41765676C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_012263.5:c.*50G= (TTLL1) MANE Select	NP_036395.1:n.*50G=
ENST00000266254.12:c.*50G= (TTLL1) MANE Select	ENSP00000266254.7:n.*50G=
NM_012263.4:c.*50G= (TTLL1)	NP_036395.1:n.*50G=
NR_027779.1:n.1667G= (TTLL1)
NR_027779.2:n.1630G= (TTLL1)
NR_125362.1:n.1142C= (TTLL1-AS1)
ENST00000266254.11:c.*50G= (TTLL1)	ENSP00000266254.7:n.*50G=
ENST00000439248.5:c.*1246G= (TTLL1)	ENSP00000401518.1:n.*1246G=
ENST00000440761.1:c.*1214G= (TTLL1)	ENSP00000403332.1:n.*1214G=
XM_006724225.2:c.*50G= (TTLL1)	XP_006724288.1:n.*50G=
XM_006724225.4:c.*50G= (TTLL1)	XP_006724288.1:n.*50G=
XM_011530108.1:c.*50G= (TTLL1)	XP_011528410.1:n.*50G=
XM_011530108.2:c.*50G= (TTLL1)	XP_011528410.1:n.*50G=
XM_011530109.1:c.*50G= (TTLL1)	XP_011528411.1:n.*50G=
XM_011530110.1:c.*50G= (TTLL1)	XP_011528412.1:n.*50G=
XM_011530110.2:c.*50G= (TTLL1)	XP_011528412.1:n.*50G=
XM_017028751.1:c.*50G= (TTLL1)	XP_016884240.1:n.*50G=
XM_017028752.1:c.*50G= (TTLL1)	XP_016884241.1:n.*50G=
XM_017028753.2:c.*50G= (TTLL1)	XP_016884242.1:n.*50G=