Canonical Allele Identifier: CA2017844112
Gene: ATF7IP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14434310G= , CM000674.2:g.14434310G= GRCh38
NC_000012.11:g.14587244G= , CM000674.1:g.14587244G= GRCh37
NC_000012.10:g.14478511G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261168.9:c.1559-27G= MANE Select ENSP00000261168.4:n.1559-27G=
ENST00000261168.8:c.1559-27G= ENSP00000261168.4:n.1559-27G=
ENST00000536444.5:c.1559-30G= ENSP00000445955.1:n.1559-30G=
ENST00000537653.5:n.1717-27G=
ENST00000538511.5:c.-125-27G= ENSP00000440587.1:n.-125-27G=
ENST00000539659.5:n.1718-30G=
ENST00000540793.5:c.1559-27G= ENSP00000444589.1:n.1559-27G=
ENST00000541654.1:n.1651-27G=
ENST00000543189.5:c.1559-30G= ENSP00000443179.1:n.1559-30G=
ENST00000544627.5:c.1583-27G= ENSP00000440440.1:n.1583-27G=
ENST00000545723.1:c.256-1885G= ENSP00000444620.1:n.256-1885G=
NM_001286514.1:c.1559-30G= NP_001273443.1:n.1559-30G=
NM_001286515.1:c.1559-30G= NP_001273444.1:n.1559-30G=
NM_018179.4:c.1559-27G= NP_060649.3:n.1559-27G=
NM_181352.1:c.1583-27G= NP_851997.1:n.1583-27G=
XM_005253424.2:c.1583-30G= XP_005253481.1:n.1583-30G=
XM_006719108.2:c.1559-27G= XP_006719171.1:n.1559-27G=
XM_006719109.2:c.1559-27G= XP_006719172.1:n.1559-27G=
XM_011520754.1:c.1559-27G= XP_011519056.1:n.1559-27G=
XM_011520755.1:c.1559-27G= XP_011519057.1:n.1559-27G=
XM_011520756.1:c.1583-27G= XP_011519058.1:n.1583-27G=
XM_011520757.1:c.1583-27G= XP_011519059.1:n.1583-27G=
XM_011520758.1:c.1583-30G= XP_011519060.1:n.1583-30G=
XM_011520759.1:c.1559-30G= XP_011519061.1:n.1559-30G=
XM_005253424.4:c.1583-30G= XP_005253481.1:n.1583-30G=
XM_006719108.3:c.1559-27G= XP_006719171.1:n.1559-27G=
XM_006719109.3:c.1559-27G= XP_006719172.1:n.1559-27G=
XM_011520754.3:c.1559-27G= XP_011519056.1:n.1559-27G=
XM_011520755.2:c.1559-27G= XP_011519057.1:n.1559-27G=
XM_011520756.3:c.1583-27G= XP_011519058.1:n.1583-27G=
XM_017019638.1:c.1559-27G= XP_016875127.1:n.1559-27G=
XM_017019639.1:c.1559-30G= XP_016875128.1:n.1559-30G=
XR_001748806.2:n.1627-27G=
XR_001748807.2:n.1627-30G=
XR_001748808.2:n.1754-27G=
XR_001748809.2:n.1754-30G=
NM_001286514.2:c.1559-30G= NP_001273443.1:n.1559-30G=
NM_001286515.2:c.1559-30G= NP_001273444.1:n.1559-30G=
NM_181352.2:c.1583-27G= NP_851997.1:n.1583-27G=
NM_001388179.1:c.1583-30G= NP_001375108.1:n.1583-30G=
NM_001388180.1:c.1559-27G= NP_001375109.1:n.1559-27G=
NM_001388181.1:c.1559-27G= NP_001375110.1:n.1559-27G=
NM_001388182.1:c.1559-27G= NP_001375111.1:n.1559-27G=
NM_001388183.1:c.1559-27G= NP_001375112.1:n.1559-27G=
NM_001388184.1:c.1559-30G= NP_001375113.1:n.1559-30G=
NM_018179.5:c.1559-27G= MANE Select NP_060649.3:n.1559-27G=
NR_170893.1:n.1712-27G=