Canonical Allele Identifier: CA384006684
Gene: ATF7IP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14434385A>C , CM000674.2:g.14434385A>C GRCh38
NC_000012.11:g.14587319A>C , CM000674.1:g.14587319A>C GRCh37
NC_000012.10:g.14478586A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261168.9:c.1607A>C MANE Select ENSP00000261168.4:p.Gln536Pro
ENST00000261168.8:c.1607A>C ENSP00000261168.4:p.Gln536Pro
ENST00000536444.5:c.1604A>C ENSP00000445955.1:p.Gln535Pro
ENST00000537653.5:n.1765A>C
ENST00000538511.5:c.-77A>C ENSP00000440587.1:n.-77A>C
ENST00000539659.5:n.1763A>C
ENST00000540793.5:c.1607A>C ENSP00000444589.1:p.Gln536Pro
ENST00000541654.1:n.1699A>C
ENST00000543189.5:c.1604A>C ENSP00000443179.1:p.Gln535Pro
ENST00000544627.5:c.1631A>C ENSP00000440440.1:p.Gln544Pro
ENST00000545723.1:c.256-1810A>C ENSP00000444620.1:n.256-1810A>C
NM_001286514.1:c.1604A>C NP_001273443.1:p.Gln535Pro
NM_001286515.1:c.1604A>C NP_001273444.1:p.Gln535Pro
NM_018179.4:c.1607A>C NP_060649.3:p.Gln536Pro
NM_181352.1:c.1631A>C NP_851997.1:p.Gln544Pro
XM_005253424.2:c.1628A>C XP_005253481.1:p.Gln543Pro
XM_006719108.2:c.1607A>C XP_006719171.1:p.Gln536Pro
XM_006719109.2:c.1607A>C XP_006719172.1:p.Gln536Pro
XM_011520754.1:c.1607A>C XP_011519056.1:p.Gln536Pro
XM_011520755.1:c.1607A>C XP_011519057.1:p.Gln536Pro
XM_011520756.1:c.1631A>C XP_011519058.1:p.Gln544Pro
XM_011520757.1:c.1631A>C XP_011519059.1:p.Gln544Pro
XM_011520758.1:c.1628A>C XP_011519060.1:p.Gln543Pro
XM_011520759.1:c.1604A>C XP_011519061.1:p.Gln535Pro
XM_005253424.4:c.1628A>C XP_005253481.1:p.Gln543Pro
XM_006719108.3:c.1607A>C XP_006719171.1:p.Gln536Pro
XM_006719109.3:c.1607A>C XP_006719172.1:p.Gln536Pro
XM_011520754.3:c.1607A>C XP_011519056.1:p.Gln536Pro
XM_011520755.2:c.1607A>C XP_011519057.1:p.Gln536Pro
XM_011520756.3:c.1631A>C XP_011519058.1:p.Gln544Pro
XM_017019638.1:c.1607A>C XP_016875127.1:p.Gln536Pro
XM_017019639.1:c.1604A>C XP_016875128.1:p.Gln535Pro
XR_001748806.2:n.1675A>C
XR_001748807.2:n.1672A>C
XR_001748808.2:n.1802A>C
XR_001748809.2:n.1799A>C
NM_001286514.2:c.1604A>C NP_001273443.1:p.Gln535Pro
NM_001286515.2:c.1604A>C NP_001273444.1:p.Gln535Pro
NM_181352.2:c.1631A>C NP_851997.1:p.Gln544Pro
NM_001388179.1:c.1628A>C NP_001375108.1:p.Gln543Pro
NM_001388180.1:c.1607A>C NP_001375109.1:p.Gln536Pro
NM_001388181.1:c.1607A>C NP_001375110.1:p.Gln536Pro
NM_001388182.1:c.1607A>C NP_001375111.1:p.Gln536Pro
NM_001388183.1:c.1607A>C NP_001375112.1:p.Gln536Pro
NM_001388184.1:c.1604A>C NP_001375113.1:p.Gln535Pro
NM_018179.5:c.1607A>C MANE Select NP_060649.3:p.Gln536Pro
NR_170893.1:n.1760A>C