Canonical Allele Identifier: CA163086212

Gene: SGCE PEG10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.94656435G>A , CM000669.2:g.94656435G>A	GRCh38
NC_000007.13:g.94285747G>A , CM000669.1:g.94285747G>A	GRCh37
NC_000007.12:g.94123683G>A	NCBI36
NG_008893.1:g.4775C>T
NG_011340.1:g.5111G>A
NG_008893.2:g.4775C>T
NG_008893.3:g.5138C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001040152.1:c.-369G>A (PEG10)	NP_001035242.1:n.-369G>A
NM_001040152.2:c.-369G>A (PEG10)	NP_001035242.1:n.-369G>A
NM_001172437.2:n.111G>A (PEG10)	NP_001165908.1:n.111G>A
NM_001172438.2:c.-152G>A (PEG10)	NP_001165909.1:n.-152G>A
NM_001172438.3:c.-152G>A (PEG10)	NP_001165909.1:n.-152G>A
NM_001184961.1:n.111G>A (PEG10)	NP_001171890.1:n.111G>A
NM_001184962.1:c.-267G>A (PEG10)	NP_001171891.1:n.-267G>A
NM_001184962.2:c.-267G>A (PEG10)	NP_001171891.1:n.-267G>A
NM_015068.3:n.111G>A (PEG10)	NP_055883.2:n.111G>A
ENST00000482108.1:c.-369G>A (PEG10)	ENSP00000417587.1:n.-369G>A
ENST00000488574.5:c.-152G>A (PEG10)	ENSP00000418944.2:n.-152G>A
ENST00000493935.1:n.66G>A (PEG10)
ENST00000612748.1:c.-152G>A (PEG10)	ENSP00000480676.1:n.-152G>A
ENST00000613043.1:c.-429G>A (PEG10)	ENSP00000482046.1:n.-429G>A
ENST00000644681.1:c.-308C>T (SGCE)	ENSP00000496455.1:n.-308C>T
ENST00000645535.1:c.-246C>T (SGCE)	ENSP00000493984.1:n.-246C>T