Canonical Allele Identifier: CA1619379778

Gene: NELFE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31952442T= , CM000668.2:g.31952442T=	GRCh38
NC_000006.11:g.31920219T= , CM000668.1:g.31920219T=	GRCh37
NC_000006.10:g.32028198T=	NCBI36
NG_008191.1:g.11499T= , LRG_136:g.11499T=

Transcript Alleles

HGVS	Amino-acid Change
NM_002904.6:c.1046-44A= MANE Select	NP_002895.3:n.1046-44A=
ENST00000375429.8:c.1046-44A= MANE Select	ENSP00000364578.3:n.1046-44A=
NM_002904.5:c.1046-44A=	NP_002895.3:n.1046-44A=
ENST00000375425.9:c.1067-44A=	ENSP00000364574.5:n.1067-44A=
ENST00000375429.7:c.1046-44A=	ENSP00000364578.3:n.1046-44A=
ENST00000444811.6:c.956-44A=	ENSP00000388400.2:n.956-44A=
ENST00000481121.5:n.1373-44A=
ENST00000488426.5:n.1685-44A=
ENST00000492185.5:n.1615-44A=
XM_006715205.2:c.1031-44A=	XP_006715268.1:n.1031-44A=
XM_006715205.3:c.1031-44A=	XP_006715268.1:n.1031-44A=
XM_011514913.1:c.881-44A=	XP_011513215.1:n.881-44A=
XM_011514913.3:c.881-44A=	XP_011513215.1:n.881-44A=
XM_017011299.2:c.866-44A=	XP_016866788.1:n.866-44A=