Canonical Allele Identifier: CA711820782

Gene: ENTREP2

Linked Data

• dbSNP Id: rs1331221599
• MyVariant Identifiers: chr15:g.29424678G>A (hg19) ; chr15:g.29132475G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.29132475G>A , CM000677.2:g.29132475G>A	GRCh38
NC_000015.9:g.29424678G>A , CM000677.1:g.29424678G>A	GRCh37
NC_000015.8:g.27211970G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261275.5:c.928-3611C>T MANE Select	ENSP00000261275.4:n.928-3611C>T
ENST00000261275.4:c.928-3611C>T	ENSP00000261275.4:n.928-3611C>T
ENST00000560021.1:n.664-3611C>T
NM_015307.1:c.928-3611C>T	NP_056122.1:n.928-3611C>T
XM_011521407.1:c.1039-3611C>T	XP_011519709.1:n.1039-3611C>T
XM_011521407.2:c.1039-3611C>T	XP_011519709.1:n.1039-3611C>T
NM_001387214.1:c.793-3611C>T	NP_001374143.1:n.793-3611C>T
NM_001387215.1:c.640-3611C>T	NP_001374144.1:n.640-3611C>T
NM_001387216.1:c.640-3611C>T	NP_001374145.1:n.640-3611C>T
NM_001387217.1:c.505-3611C>T	NP_001374146.1:n.505-3611C>T
NM_015307.2:c.928-3611C>T MANE Select	NP_056122.1:n.928-3611C>T