Canonical Allele Identifier: CA349278970

Gene: DCAF17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171476865T>A , CM000664.2:g.171476865T>A	GRCh38
NC_000002.11:g.172333375T>A , CM000664.1:g.172333375T>A	GRCh37
NC_000002.10:g.172041621T>A	NCBI36
NG_013038.1:g.47615T>A
NG_013038.2:g.47615T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025000.4:c.1097T>A MANE Select	NP_079276.2:p.Leu366Ter
ENST00000375255.8:c.1097T>A MANE Select	ENSP00000364404.3:p.Leu366Ter
NM_001164821.1:c.982-1122T>A	NP_001158293.1:n.982-1122T>A
NM_001164821.2:c.982-1122T>A	NP_001158293.1:n.982-1122T>A
NM_025000.3:c.1097T>A	NP_079276.2:p.Leu366Ter
NR_028482.1:n.1318T>A
NR_028482.2:n.1343T>A
ENST00000339506.7:c.349T>A
ENST00000375255.7:c.1097T>A	ENSP00000364404.3:p.Leu366Ter
ENST00000431110.1:c.202T>A
ENST00000468592.5:n.919T>A
ENST00000539783.5:c.982-1122T>A	ENSP00000442238.1:n.982-1122T>A
ENST00000611110.4:c.257T>A	ENSP00000477604.1:p.Leu86Ter
XM_006712766.2:c.1097T>A	XP_006712829.1:p.Leu366Ter
XM_006712767.1:c.836T>A	XP_006712830.1:p.Leu279Ter
XM_006712768.1:c.836T>A	XP_006712831.1:p.Leu279Ter
XM_006712772.2:c.*15-1122T>A	XP_006712835.1:n.*15-1122T>A
XM_006712773.2:c.419T>A	XP_006712836.1:p.Leu140Ter
XM_011511881.1:c.1064T>A	XP_011510183.1:p.Leu355Ter
XM_011511882.1:c.1034T>A	XP_011510184.1:p.Leu345Ter
XM_011511883.1:c.981+7835T>A	XP_011510185.1:n.981+7835T>A
XM_011511884.1:c.*14+7835T>A	XP_011510186.1:n.*14+7835T>A
XM_017004995.1:c.1091+2890T>A	XP_016860484.1:n.1091+2890T>A
XM_017004997.1:c.987T>A	XP_016860486.1:p.Phe329Leu
XM_017004998.1:c.419T>A	XP_016860487.1:p.Leu140Ter
XM_017004999.1:c.*20T>A	XP_016860488.1:n.*20T>A
XM_017005002.1:c.356T>A	XP_016860491.1:p.Leu119Ter
XR_001738961.1:n.1198-1122T>A
XR_427113.2:n.1203T>A
XR_923029.1:n.1309T>A
XR_923030.1:n.1309T>A