Canonical Allele Identifier: CA349278829

Gene: DCAF17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171473922T>G , CM000664.2:g.171473922T>G	GRCh38
NC_000002.11:g.172330432T>G , CM000664.1:g.172330432T>G	GRCh37
NC_000002.10:g.172038678T>G	NCBI36
NG_013038.1:g.44672T>G
NG_013038.2:g.44672T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025000.4:c.1038T>G MANE Select	NP_079276.2:p.Tyr346Ter
ENST00000375255.8:c.1038T>G MANE Select	ENSP00000364404.3:p.Tyr346Ter
NM_001164821.1:c.982-4065T>G	NP_001158293.1:n.982-4065T>G
NM_001164821.2:c.982-4065T>G	NP_001158293.1:n.982-4065T>G
NM_025000.3:c.1038T>G	NP_079276.2:p.Tyr346Ter
NR_028482.1:n.1259T>G
NR_028482.2:n.1284T>G
ENST00000339506.7:c.290T>G
ENST00000375255.7:c.1038T>G	ENSP00000364404.3:p.Tyr346Ter
ENST00000431110.1:c.143T>G
ENST00000468592.5:n.860T>G
ENST00000493106.1:n.111T>G
ENST00000539783.5:c.982-4065T>G	ENSP00000442238.1:n.982-4065T>G
ENST00000611110.4:c.198T>G	ENSP00000477604.1:p.Tyr66Ter
XM_006712766.2:c.1038T>G	XP_006712829.1:p.Tyr346Ter
XM_006712767.1:c.777T>G	XP_006712830.1:p.Tyr259Ter
XM_006712768.1:c.777T>G	XP_006712831.1:p.Tyr259Ter
XM_006712772.2:c.*15-4065T>G	XP_006712835.1:n.*15-4065T>G
XM_006712773.2:c.360T>G	XP_006712836.1:p.Tyr120Ter
XM_011511881.1:c.1005T>G	XP_011510183.1:p.Tyr335Ter
XM_011511882.1:c.975T>G	XP_011510184.1:p.Tyr325Ter
XM_011511883.1:c.981+4892T>G	XP_011510185.1:n.981+4892T>G
XM_011511884.1:c.*14+4892T>G	XP_011510186.1:n.*14+4892T>G
XM_017004995.1:c.1038T>G	XP_016860484.1:p.Tyr346Ter
XM_017004997.1:c.982-2938T>G	XP_016860486.1:n.982-2938T>G
XM_017004998.1:c.360T>G	XP_016860487.1:p.Tyr120Ter
XM_017004999.1:c.*15-2938T>G	XP_016860488.1:n.*15-2938T>G
XM_017005000.1:c.*71T>G	XP_016860489.1:n.*71T>G
XM_017005002.1:c.297T>G	XP_016860491.1:p.Tyr99Ter
XR_001738961.1:n.1198-4065T>G
XR_427113.2:n.1198-2938T>G
XR_923029.1:n.1304-2938T>G
XR_923030.1:n.1304-2938T>G