Canonical Allele Identifier: CA2017885550
Gene: ATF7IP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14500992_14500993delinsCA , CM000674.2:g.14500992_14500993delinsCA GRCh38
NC_000012.11:g.14653926_14653927delinsCA , CM000674.1:g.14653926_14653927delinsCA GRCh37
NC_000012.10:g.14545193_14545194delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261168.9:c.*2919_*2920delinsCA MANE Select ENSP00000261168.4:n.*2919_*2920delinsCA
ENST00000261168.8:c.*2919_*2920delinsCA ENSP00000261168.4:n.*2919_*2920delinsCA
ENST00000536444.5:c.*2919_*2920delinsCA ENSP00000445955.1:n.*2919_*2920delinsCA
NM_001286514.1:c.*2919_*2920delinsCA NP_001273443.1:n.*2919_*2920delinsCA
NM_018179.4:c.*2919_*2920delinsCA NP_060649.3:n.*2919_*2920delinsCA
NM_181352.1:c.*2919_*2920delinsCA NP_851997.1:n.*2919_*2920delinsCA
XM_005253424.4:c.*2919_*2920delinsCA XP_005253481.1:n.*2919_*2920delinsCA
XM_006719108.3:c.*2919_*2920delinsCA XP_006719171.1:n.*2919_*2920delinsCA
XM_006719109.3:c.*2919_*2920delinsCA XP_006719172.1:n.*2919_*2920delinsCA
XM_011520754.3:c.*2919_*2920delinsCA XP_011519056.1:n.*2919_*2920delinsCA
XM_011520755.2:c.*2919_*2920delinsCA XP_011519057.1:n.*2919_*2920delinsCA
XM_017019638.1:c.*2919_*2920delinsCA XP_016875127.1:n.*2919_*2920delinsCA
XM_017019639.1:c.*2919_*2920delinsCA XP_016875128.1:n.*2919_*2920delinsCA
XR_001748808.2:n.6838_6839delinsCA
NM_001286514.2:c.*2919_*2920delinsCA NP_001273443.1:n.*2919_*2920delinsCA
NM_181352.2:c.*2919_*2920delinsCA NP_851997.1:n.*2919_*2920delinsCA
NM_001388179.1:c.*2919_*2920delinsCA NP_001375108.1:n.*2919_*2920delinsCA
NM_001388180.1:c.*2919_*2920delinsCA NP_001375109.1:n.*2919_*2920delinsCA
NM_001388181.1:c.*2919_*2920delinsCA NP_001375110.1:n.*2919_*2920delinsCA
NM_001388182.1:c.*2919_*2920delinsCA NP_001375111.1:n.*2919_*2920delinsCA
NM_001388183.1:c.*2919_*2920delinsCA NP_001375112.1:n.*2919_*2920delinsCA
NM_001388184.1:c.*2919_*2920delinsCA NP_001375113.1:n.*2919_*2920delinsCA
NM_018179.5:c.*2919_*2920delinsCA MANE Select NP_060649.3:n.*2919_*2920delinsCA
NR_170893.1:n.6796_6797delinsCA