Canonical Allele Identifier: CA384006740
Gene: ATF7IP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14434402G>A , CM000674.2:g.14434402G>A GRCh38
NC_000012.11:g.14587336G>A , CM000674.1:g.14587336G>A GRCh37
NC_000012.10:g.14478603G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261168.9:c.1624G>A MANE Select ENSP00000261168.4:p.Asp542Asn
ENST00000261168.8:c.1624G>A ENSP00000261168.4:p.Asp542Asn
ENST00000536444.5:c.1621G>A ENSP00000445955.1:p.Asp541Asn
ENST00000537653.5:n.1782G>A
ENST00000538511.5:c.-60G>A ENSP00000440587.1:n.-60G>A
ENST00000539659.5:n.1780G>A
ENST00000540793.5:c.1624G>A ENSP00000444589.1:p.Asp542Asn
ENST00000541654.1:n.1716G>A
ENST00000543189.5:c.1621G>A ENSP00000443179.1:p.Asp541Asn
ENST00000544627.5:c.1648G>A ENSP00000440440.1:p.Asp550Asn
ENST00000545723.1:c.256-1793G>A ENSP00000444620.1:n.256-1793G>A
NM_001286514.1:c.1621G>A NP_001273443.1:p.Asp541Asn
NM_001286515.1:c.1621G>A NP_001273444.1:p.Asp541Asn
NM_018179.4:c.1624G>A NP_060649.3:p.Asp542Asn
NM_181352.1:c.1648G>A NP_851997.1:p.Asp550Asn
XM_005253424.2:c.1645G>A XP_005253481.1:p.Asp549Asn
XM_006719108.2:c.1624G>A XP_006719171.1:p.Asp542Asn
XM_006719109.2:c.1624G>A XP_006719172.1:p.Asp542Asn
XM_011520754.1:c.1624G>A XP_011519056.1:p.Asp542Asn
XM_011520755.1:c.1624G>A XP_011519057.1:p.Asp542Asn
XM_011520756.1:c.1648G>A XP_011519058.1:p.Asp550Asn
XM_011520757.1:c.1648G>A XP_011519059.1:p.Asp550Asn
XM_011520758.1:c.1645G>A XP_011519060.1:p.Asp549Asn
XM_011520759.1:c.1621G>A XP_011519061.1:p.Asp541Asn
XM_005253424.4:c.1645G>A XP_005253481.1:p.Asp549Asn
XM_006719108.3:c.1624G>A XP_006719171.1:p.Asp542Asn
XM_006719109.3:c.1624G>A XP_006719172.1:p.Asp542Asn
XM_011520754.3:c.1624G>A XP_011519056.1:p.Asp542Asn
XM_011520755.2:c.1624G>A XP_011519057.1:p.Asp542Asn
XM_011520756.3:c.1648G>A XP_011519058.1:p.Asp550Asn
XM_017019638.1:c.1624G>A XP_016875127.1:p.Asp542Asn
XM_017019639.1:c.1621G>A XP_016875128.1:p.Asp541Asn
XR_001748806.2:n.1692G>A
XR_001748807.2:n.1689G>A
XR_001748808.2:n.1819G>A
XR_001748809.2:n.1816G>A
NM_001286514.2:c.1621G>A NP_001273443.1:p.Asp541Asn
NM_001286515.2:c.1621G>A NP_001273444.1:p.Asp541Asn
NM_181352.2:c.1648G>A NP_851997.1:p.Asp550Asn
NM_001388179.1:c.1645G>A NP_001375108.1:p.Asp549Asn
NM_001388180.1:c.1624G>A NP_001375109.1:p.Asp542Asn
NM_001388181.1:c.1624G>A NP_001375110.1:p.Asp542Asn
NM_001388182.1:c.1624G>A NP_001375111.1:p.Asp542Asn
NM_001388183.1:c.1624G>A NP_001375112.1:p.Asp542Asn
NM_001388184.1:c.1621G>A NP_001375113.1:p.Asp541Asn
NM_018179.5:c.1624G>A MANE Select NP_060649.3:p.Asp542Asn
NR_170893.1:n.1777G>A