Canonical Allele Identifier: CA2838462793

Gene: ZKSCAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100023460del , CM000669.2:g.100023460del	GRCh38
NC_000007.13:g.99621083del , CM000669.1:g.99621083del	GRCh37
NC_000007.12:g.99459019del	NCBI36
NG_051950.1:g.12909del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324306.11:c.-47del MANE Select	ENSP00000323148.6:n.-47del
ENST00000324306.10:c.-47del	ENSP00000323148.6:n.-47del
ENST00000426572.5:c.-65del	ENSP00000409172.1:n.-65del
ENST00000432317.1:c.-47del	ENSP00000394445.1:n.-47del
ENST00000482979.5:n.170del
ENST00000535170.5:c.-59-6401del	ENSP00000443508.1:n.-59-6401del
ENST00000620510.1:c.-65del	ENSP00000480305.1:n.-65del
NM_001287054.1:c.-65del	NP_001273983.1:n.-65del
NM_001287055.1:c.-59-6401del	NP_001273984.1:n.-59-6401del
NM_003439.2:c.-47del	NP_003430.1:n.-47del
XM_005250565.3:c.-47del	XP_005250622.1:n.-47del
XM_011516559.1:c.-47del	XP_011514861.1:n.-47del
XR_927529.1:n.188del
NM_001287054.2:c.-65del	NP_001273983.1:n.-65del
NM_001287055.2:c.-59-6401del	NP_001273984.1:n.-59-6401del
NM_001346579.1:c.-47del	NP_001333508.1:n.-47del
NM_001346580.1:c.-65del	NP_001333509.1:n.-65del
NM_001346581.1:c.-47del	NP_001333510.1:n.-47del
NM_003439.3:c.-47del	NP_003430.1:n.-47del
NR_144477.1:n.217del
XM_011516559.3:c.-47del	XP_011514861.1:n.-47del
XR_002956485.1:n.188del
XR_927529.2:n.188del
NM_003439.4:c.-47del MANE Select	NP_003430.1:n.-47del
NM_001287054.3:c.-65del	NP_001273983.1:n.-65del
NM_001346580.2:c.-65del	NP_001333509.1:n.-65del
NM_001346581.2:c.-47del	NP_001333510.1:n.-47del
NR_144477.2:n.173del
NM_001287055.3:c.-59-6401del	NP_001273984.1:n.-59-6401del
NM_001346579.2:c.-47del	NP_001333508.1:n.-47del