Canonical Allele Identifier: CA2838538751

Gene: CECR2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17461026T>C , CM000684.2:g.17461026T>C	GRCh38
NC_000022.10:g.17940063T>C , CM000684.1:g.17940063T>C	GRCh37
NC_000022.9:g.16320063T>C	NCBI36
NG_033989.1:g.106078T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262608.13:c.127-16562T>C MANE Select	ENSP00000262608.11:n.127-16562T>C
ENST00000342247.10:c.127-16562T>C	ENSP00000341219.6:n.127-16562T>C
ENST00000400585.7:c.-363-16562T>C	ENSP00000383428.2:n.-363-16562T>C
ENST00000262608.12:c.-363-16562T>C	ENSP00000262608.10:n.-363-16562T>C
ENST00000342247.9:c.127-16562T>C	ENSP00000341219.6:n.127-16562T>C
ENST00000400585.6:c.-363-16562T>C	ENSP00000383428.2:n.-363-16562T>C
ENST00000497534.1:n.269-16562T>C
NM_001290046.1:c.-363-16562T>C	NP_001276975.1:n.-363-16562T>C
NM_001290047.1:c.127-16562T>C	NP_001276976.1:n.127-16562T>C
XM_011546128.1:c.127-16562T>C	XP_011544430.1:n.127-16562T>C
XM_011546129.1:c.127-16562T>C	XP_011544431.1:n.127-16562T>C
XM_011546130.1:c.12+5895T>C	XP_011544432.1:n.12+5895T>C
XM_011546131.1:c.4-16562T>C	XP_011544433.1:n.4-16562T>C
XM_011546132.1:c.127-16562T>C	XP_011544434.1:n.127-16562T>C
XR_951200.1:n.206-16562T>C
XR_951201.1:n.205-16562T>C
XM_011546128.2:c.127-16562T>C	XP_011544430.1:n.127-16562T>C
XM_011546129.2:c.127-16562T>C	XP_011544431.1:n.127-16562T>C
XM_011546132.2:c.127-16562T>C	XP_011544434.1:n.127-16562T>C
XM_017028785.1:c.127-16562T>C	XP_016884274.1:n.127-16562T>C
XR_951200.2:n.233-16562T>C
XR_951201.2:n.233-16562T>C
NM_001290047.2:c.127-16562T>C MANE Select	NP_001276976.1:n.127-16562T>C
NM_001290046.2:c.-363-16562T>C	NP_001276975.1:n.-363-16562T>C