Canonical Allele Identifier: CA1565186118

Gene: ELL2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.95899087C>G , CM000667.2:g.95899087C>G	GRCh38
NC_000005.9:g.95234791C>G , CM000667.1:g.95234791C>G	GRCh37
NC_000005.8:g.95260547C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237853.9:c.955-277G>C MANE Select	ENSP00000237853.4:n.955-277G>C
ENST00000237853.8:c.955-277G>C	ENSP00000237853.4:n.955-277G>C
ENST00000513343.1:c.409-277G>C	ENSP00000423915.1:n.409-277G>C
NM_012081.5:c.955-277G>C	NP_036213.2:n.955-277G>C
XM_006714575.1:c.790-277G>C	XP_006714638.1:n.790-277G>C
XM_011543280.1:c.559-277G>C	XP_011541582.1:n.559-277G>C
XM_006714575.3:c.790-277G>C	XP_006714638.1:n.790-277G>C
XM_017009239.1:c.955-277G>C	XP_016864728.1:n.955-277G>C
XM_017009240.2:c.559-277G>C	XP_016864729.1:n.559-277G>C
XM_017009241.2:c.559-277G>C	XP_016864730.1:n.559-277G>C
XM_017009242.1:c.559-277G>C	XP_016864731.1:n.559-277G>C
XM_017009243.2:c.400-277G>C	XP_016864732.1:n.400-277G>C
NM_012081.6:c.955-277G>C MANE Select	NP_036213.2:n.955-277G>C