Canonical Allele Identifier: CA5675143

Gene: NEURL1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103571760C>T , CM000672.2:g.103571760C>T	GRCh38
NC_000010.10:g.105331517C>T , CM000672.1:g.105331517C>T	GRCh37
NC_000010.9:g.105321507C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369780.9:c.587C>T MANE Select	ENSP00000358795.4:p.Thr196Met
ENST00000369780.8:c.587C>T	ENSP00000358795.4:p.Thr196Met
ENST00000437579.1:c.536C>T	ENSP00000416709.1:p.Thr179Met
ENST00000465048.1:n.84C>T
NM_004210.4:c.587C>T	NP_004201.3:p.Thr196Met
XM_005270269.2:c.536C>T	XP_005270326.1:p.Thr179Met
XM_005270270.2:c.362C>T	XP_005270327.1:p.Thr121Met
XM_011540331.1:c.701C>T	XP_011538633.1:p.Thr234Met
XM_011540332.1:c.647C>T	XP_011538634.1:p.Thr216Met
XM_011540333.1:c.533C>T	XP_011538635.1:p.Thr178Met
XM_011540334.1:c.362C>T	XP_011538636.1:p.Thr121Met
XM_011540335.1:c.701C>T	XP_011538637.1:p.Thr234Met
XR_945866.1:n.1199C>T
XM_005270269.4:c.536C>T	XP_005270326.1:p.Thr179Met
XM_005270270.4:c.362C>T	XP_005270327.1:p.Thr121Met
XM_011540331.3:c.701C>T	XP_011538633.1:p.Thr234Met
XM_011540332.2:c.647C>T	XP_011538634.1:p.Thr216Met
XM_011540333.2:c.533C>T	XP_011538635.1:p.Thr178Met
XM_011540335.3:c.701C>T	XP_011538637.1:p.Thr234Met
XM_017016909.2:c.605C>T	XP_016872398.1:p.Thr202Met
XR_945866.2:n.1301C>T
NM_004210.5:c.587C>T MANE Select	NP_004201.3:p.Thr196Met