Canonical Allele Identifier: CA1510302650

Gene: TLL1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.165909327C= , CM000666.2:g.165909327C=	GRCh38
NC_000004.11:g.166830479C= , CM000666.1:g.166830479C=	GRCh37
NC_000004.10:g.167049929C=	NCBI36
NG_016278.1:g.41070C=
NG_016278.2:g.41070C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000061240.7:c.169+35254C= MANE Select	ENSP00000061240.2:n.169+35254C=
ENST00000061240.6:c.169+35254C=	ENSP00000061240.2:n.169+35254C=
ENST00000504560.5:c.170-10507C=	ENSP00000421732.1:n.170-10507C=
ENST00000506144.1:c.-132+34275C=	ENSP00000423748.1:n.-132+34275C=
ENST00000507499.5:c.169+35254C=	ENSP00000426082.1:n.169+35254C=
ENST00000509505.5:c.169+35254C=	ENSP00000422692.1:n.169+35254C=
ENST00000513213.5:c.169+35254C=	ENSP00000422937.1:n.169+35254C=
NM_001204760.1:c.169+35254C=	NP_001191689.1:n.169+35254C=
NM_012464.4:c.169+35254C=	NP_036596.3:n.169+35254C=
XM_011532212.1:c.169+35254C=	XP_011530514.1:n.169+35254C=
XM_011532213.1:c.-84-10507C=	XP_011530515.1:n.-84-10507C=
XM_011532214.1:c.-398+35254C=	XP_011530516.1:n.-398+35254C=
XM_017008570.1:c.-84-10507C=	XP_016864059.1:n.-84-10507C=
XM_024454194.1:c.-132+36185C=	XP_024309962.1:n.-132+36185C=
NM_012464.5:c.169+35254C= MANE Select	NP_036596.3:n.169+35254C=
NM_001204760.2:c.169+35254C=	NP_001191689.1:n.169+35254C=