Canonical Allele Identifier: CA14128726

Gene: ENTREP2

Linked Data

• dbSNP Id: rs4780054
• gnomAD v2: 15-29600003-C-T
• gnomAD v3: 15-29307799-C-T
• gnomAD v4: 15-29307799-C-T
• MyVariant Identifiers: chr15:g.29600003C>T (hg19) ; chr15:g.29307799C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.29307799C>T , CM000677.2:g.29307799C>T	GRCh38
NC_000015.9:g.29600003C>T , CM000677.1:g.29600003C>T	GRCh37
NC_000015.8:g.27387295C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261275.5:c.277-55321G>A MANE Select	ENSP00000261275.4:n.277-55321G>A
ENST00000261275.4:c.277-55321G>A	ENSP00000261275.4:n.277-55321G>A
ENST00000560082.1:c.-12-55321G>A	ENSP00000452860.1:n.-12-55321G>A
NM_015307.1:c.277-55321G>A	NP_056122.1:n.277-55321G>A
XM_011521407.1:c.160-55321G>A	XP_011519709.1:n.160-55321G>A
XM_011521407.2:c.160-55321G>A	XP_011519709.1:n.160-55321G>A
NM_001387214.1:c.277-55321G>A	NP_001374143.1:n.277-55321G>A
NM_001387215.1:c.-12-55321G>A	NP_001374144.1:n.-12-55321G>A
NM_001387216.1:c.-12-55321G>A	NP_001374145.1:n.-12-55321G>A
NM_001387217.1:c.-12-55321G>A	NP_001374146.1:n.-12-55321G>A
NM_015307.2:c.277-55321G>A MANE Select	NP_056122.1:n.277-55321G>A