Canonical Allele Identifier: CA1463667780

Gene: TECRL

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.64304697C= , CM000666.2:g.64304697C=	GRCh38
NC_000004.11:g.65170415C= , CM000666.1:g.65170415C=	GRCh37
NC_000004.10:g.64853010C=	NCBI36
NG_053152.1:g.109813G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381210.8:c.730+469G= MANE Select	ENSP00000370607.3:n.730+469G=
ENST00000381210.7:c.730+469G=	ENSP00000370607.3:n.730+469G=
ENST00000507440.5:c.730+469G=	ENSP00000426043.1:n.730+469G=
ENST00000513125.5:n.303+469G=
NM_001010874.4:c.730+469G=	NP_001010874.2:n.730+469G=
XM_005265662.3:c.685+469G=	XP_005265719.1:n.685+469G=
XM_005265663.2:c.730+469G=	XP_005265720.1:n.730+469G=
XM_005265664.2:c.730+469G=	XP_005265721.1:n.730+469G=
XM_005265665.2:c.730+469G=	XP_005265722.1:n.730+469G=
NM_001363796.1:c.730+469G=	NP_001350725.1:n.730+469G=
XM_005265662.5:c.685+469G=	XP_005265719.1:n.685+469G=
XM_005265664.3:c.730+469G=	XP_005265721.1:n.730+469G=
XM_005265665.4:c.730+469G=	XP_005265722.1:n.730+469G=
XM_017007959.2:c.730+469G=	XP_016863448.1:n.730+469G=
XM_024453961.1:c.685+469G=	XP_024309729.1:n.685+469G=
XM_024453962.1:c.685+469G=	XP_024309730.1:n.685+469G=
NM_001010874.5:c.730+469G= MANE Select	NP_001010874.2:n.730+469G=