Canonical Allele Identifier: CA98615652

Gene: TECRL

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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