Canonical Allele Identifier: CA2017844138
Gene: ATF7IP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14434393C= , CM000674.2:g.14434393C= GRCh38
NC_000012.11:g.14587327C= , CM000674.1:g.14587327C= GRCh37
NC_000012.10:g.14478594C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261168.9:c.1615C= MANE Select ENSP00000261168.4:p.His539=
ENST00000261168.8:c.1615C= ENSP00000261168.4:p.His539=
ENST00000536444.5:c.1612C= ENSP00000445955.1:p.His538=
ENST00000537653.5:n.1773C=
ENST00000538511.5:c.-69C= ENSP00000440587.1:n.-69C=
ENST00000539659.5:n.1771C=
ENST00000540793.5:c.1615C= ENSP00000444589.1:p.His539=
ENST00000541654.1:n.1707C=
ENST00000543189.5:c.1612C= ENSP00000443179.1:p.His538=
ENST00000544627.5:c.1639C= ENSP00000440440.1:p.His547=
ENST00000545723.1:c.256-1802C= ENSP00000444620.1:n.256-1802C=
NM_001286514.1:c.1612C= NP_001273443.1:p.His538=
NM_001286515.1:c.1612C= NP_001273444.1:p.His538=
NM_018179.4:c.1615C= NP_060649.3:p.His539=
NM_181352.1:c.1639C= NP_851997.1:p.His547=
XM_005253424.2:c.1636C= XP_005253481.1:p.His546=
XM_006719108.2:c.1615C= XP_006719171.1:p.His539=
XM_006719109.2:c.1615C= XP_006719172.1:p.His539=
XM_011520754.1:c.1615C= XP_011519056.1:p.His539=
XM_011520755.1:c.1615C= XP_011519057.1:p.His539=
XM_011520756.1:c.1639C= XP_011519058.1:p.His547=
XM_011520757.1:c.1639C= XP_011519059.1:p.His547=
XM_011520758.1:c.1636C= XP_011519060.1:p.His546=
XM_011520759.1:c.1612C= XP_011519061.1:p.His538=
XM_005253424.4:c.1636C= XP_005253481.1:p.His546=
XM_006719108.3:c.1615C= XP_006719171.1:p.His539=
XM_006719109.3:c.1615C= XP_006719172.1:p.His539=
XM_011520754.3:c.1615C= XP_011519056.1:p.His539=
XM_011520755.2:c.1615C= XP_011519057.1:p.His539=
XM_011520756.3:c.1639C= XP_011519058.1:p.His547=
XM_017019638.1:c.1615C= XP_016875127.1:p.His539=
XM_017019639.1:c.1612C= XP_016875128.1:p.His538=
XR_001748806.2:n.1683C=
XR_001748807.2:n.1680C=
XR_001748808.2:n.1810C=
XR_001748809.2:n.1807C=
NM_001286514.2:c.1612C= NP_001273443.1:p.His538=
NM_001286515.2:c.1612C= NP_001273444.1:p.His538=
NM_181352.2:c.1639C= NP_851997.1:p.His547=
NM_001388179.1:c.1636C= NP_001375108.1:p.His546=
NM_001388180.1:c.1615C= NP_001375109.1:p.His539=
NM_001388181.1:c.1615C= NP_001375110.1:p.His539=
NM_001388182.1:c.1615C= NP_001375111.1:p.His539=
NM_001388183.1:c.1615C= NP_001375112.1:p.His539=
NM_001388184.1:c.1612C= NP_001375113.1:p.His538=
NM_018179.5:c.1615C= MANE Select NP_060649.3:p.His539=
NR_170893.1:n.1768C=