Canonical Allele Identifier: CA14400789

Gene: AATF

Linked Data

• dbSNP Id: rs2306658
• gnomAD v2: 17-35306312-G-C
• gnomAD v3: 17-36949012-G-C
• gnomAD v4: 17-36949012-G-C
• MyVariant Identifiers: chr17:g.35306312G>C (hg19) ; chr17:g.36949012G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.36949012G>C , CM000679.2:g.36949012G>C	GRCh38
NC_000017.10:g.35306312G>C , CM000679.1:g.35306312G>C	GRCh37
NC_000017.9:g.32380425G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000616434.2:c.-114G>C	ENSP00000477881.2:n.-114G>C
ENST00000619387.5:c.-114G>C MANE Select	ENSP00000477848.1:n.-114G>C
ENST00000679508.1:n.88G>C
ENST00000679985.1:n.88G>C
ENST00000679997.1:c.-114G>C	ENSP00000505070.1:n.-114G>C
ENST00000680330.1:c.-114G>C	ENSP00000506539.1:n.-114G>C
ENST00000680340.1:c.-114G>C	ENSP00000506264.1:n.-114G>C
ENST00000680356.1:c.-114G>C	ENSP00000505146.1:n.-114G>C
ENST00000680579.1:c.-114G>C	ENSP00000506655.1:n.-114G>C
ENST00000680807.1:n.88G>C
ENST00000681070.1:n.46G>C
ENST00000681800.1:n.88G>C
ENST00000619387.4:c.-114G>C	ENSP00000477848.1:n.-114G>C
NM_012138.3:c.-114G>C	NP_036270.1:n.-114G>C
XM_011524611.1:c.-114G>C	XP_011522913.1:n.-114G>C
XR_934439.1:n.122G>C
XM_011524611.2:c.-114G>C	XP_011522913.1:n.-114G>C
XR_934439.3:n.59G>C
NM_012138.4:c.-114G>C MANE Select	NP_036270.1:n.-114G>C