Canonical Allele Identifier: CA2842140012

Gene: ATF7IP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14501028T>C , CM000674.2:g.14501028T>C	GRCh38
NC_000012.11:g.14653962T>C , CM000674.1:g.14653962T>C	GRCh37
NC_000012.10:g.14545229T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261168.9:c.*2955T>C MANE Select	ENSP00000261168.4:n.*2955T>C
ENST00000261168.8:c.*2955T>C	ENSP00000261168.4:n.*2955T>C
ENST00000536444.5:c.*2955T>C	ENSP00000445955.1:n.*2955T>C
NM_001286514.1:c.*2955T>C	NP_001273443.1:n.*2955T>C
NM_018179.4:c.*2955T>C	NP_060649.3:n.*2955T>C
NM_181352.1:c.*2955T>C	NP_851997.1:n.*2955T>C
XM_005253424.4:c.*2955T>C	XP_005253481.1:n.*2955T>C
XM_006719108.3:c.*2955T>C	XP_006719171.1:n.*2955T>C
XM_006719109.3:c.*2955T>C	XP_006719172.1:n.*2955T>C
XM_011520754.3:c.*2955T>C	XP_011519056.1:n.*2955T>C
XM_011520755.2:c.*2955T>C	XP_011519057.1:n.*2955T>C
XM_017019638.1:c.*2955T>C	XP_016875127.1:n.*2955T>C
XM_017019639.1:c.*2955T>C	XP_016875128.1:n.*2955T>C
XR_001748808.2:n.6874T>C
NM_001286514.2:c.*2955T>C	NP_001273443.1:n.*2955T>C
NM_181352.2:c.*2955T>C	NP_851997.1:n.*2955T>C
NM_001388179.1:c.*2955T>C	NP_001375108.1:n.*2955T>C
NM_001388180.1:c.*2955T>C	NP_001375109.1:n.*2955T>C
NM_001388181.1:c.*2955T>C	NP_001375110.1:n.*2955T>C
NM_001388182.1:c.*2955T>C	NP_001375111.1:n.*2955T>C
NM_001388183.1:c.*2955T>C	NP_001375112.1:n.*2955T>C
NM_001388184.1:c.*2955T>C	NP_001375113.1:n.*2955T>C
NM_018179.5:c.*2955T>C MANE Select	NP_060649.3:n.*2955T>C
NR_170893.1:n.6832T>C