Canonical Allele Identifier: CA349278956

Gene: DCAF17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171476858A>G , CM000664.2:g.171476858A>G	GRCh38
NC_000002.11:g.172333368A>G , CM000664.1:g.172333368A>G	GRCh37
NC_000002.10:g.172041614A>G	NCBI36
NG_013038.1:g.47608A>G
NG_013038.2:g.47608A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025000.4:c.1092-2A>G MANE Select	NP_079276.2:n.1092-2A>G
ENST00000375255.8:c.1092-2A>G MANE Select	ENSP00000364404.3:n.1092-2A>G
NM_001164821.1:c.982-1129A>G	NP_001158293.1:n.982-1129A>G
NM_001164821.2:c.982-1129A>G	NP_001158293.1:n.982-1129A>G
NM_025000.3:c.1092-2A>G	NP_079276.2:n.1092-2A>G
NR_028482.1:n.1313-2A>G
NR_028482.2:n.1338-2A>G
ENST00000339506.7:c.344-2A>G
ENST00000375255.7:c.1092-2A>G	ENSP00000364404.3:n.1092-2A>G
ENST00000431110.1:c.197-2A>G
ENST00000468592.5:n.914-2A>G
ENST00000539783.5:c.982-1129A>G	ENSP00000442238.1:n.982-1129A>G
ENST00000611110.4:c.252-2A>G	ENSP00000477604.1:n.252-2A>G
XM_006712766.2:c.1092-2A>G	XP_006712829.1:n.1092-2A>G
XM_006712767.1:c.831-2A>G	XP_006712830.1:n.831-2A>G
XM_006712768.1:c.831-2A>G	XP_006712831.1:n.831-2A>G
XM_006712772.2:c.*15-1129A>G	XP_006712835.1:n.*15-1129A>G
XM_006712773.2:c.414-2A>G	XP_006712836.1:n.414-2A>G
XM_011511881.1:c.1059-2A>G	XP_011510183.1:n.1059-2A>G
XM_011511882.1:c.1029-2A>G	XP_011510184.1:n.1029-2A>G
XM_011511883.1:c.981+7828A>G	XP_011510185.1:n.981+7828A>G
XM_011511884.1:c.*14+7828A>G	XP_011510186.1:n.*14+7828A>G
XM_017004995.1:c.1091+2883A>G	XP_016860484.1:n.1091+2883A>G
XM_017004997.1:c.982-2A>G	XP_016860486.1:n.982-2A>G
XM_017004998.1:c.414-2A>G	XP_016860487.1:n.414-2A>G
XM_017004999.1:c.*15-2A>G	XP_016860488.1:n.*15-2A>G
XM_017005002.1:c.351-2A>G	XP_016860491.1:n.351-2A>G
XR_001738961.1:n.1198-1129A>G
XR_427113.2:n.1198-2A>G
XR_923029.1:n.1304-2A>G
XR_923030.1:n.1304-2A>G