Canonical Allele Identifier: CA413412273

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64141776T>G (hg19) ; chrX:g.64921896T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921896T>G , CM000685.2:g.64921896T>G	GRCh38
NC_000023.10:g.64141776T>G , CM000685.1:g.64141776T>G	GRCh37
NC_000023.9:g.64058501T>G	NCBI36
NG_021200.1:g.59638A>C
NG_021200.2:g.117849A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.77A>C	ENSP00000515193.1:p.Lys26Thr
ENST00000492653.6:c.146A>C	ENSP00000515192.1:p.Lys49Thr
ENST00000703133.1:c.*720A>C	ENSP00000515188.1:n.*720A>C
ENST00000703136.1:c.*104A>C	ENSP00000515190.1:n.*104A>C
ENST00000374839.8:c.146A>C MANE Select	ENSP00000363972.3:p.Lys49Thr
ENST00000337990.2:c.77A>C	ENSP00000338650.2:p.Lys26Thr
ENST00000374839.7:c.146A>C	ENSP00000363972.3:p.Lys49Thr
ENST00000447788.6:c.146A>C	ENSP00000399126.2:p.Lys49Thr
ENST00000476032.1:n.387A>C
ENST00000488608.5:n.302A>C
ENST00000488831.5:n.134A>C
ENST00000492653.5:n.242A>C
NM_001178032.2:c.77A>C	NP_001171503.1:p.Lys26Thr
NM_001178033.2:c.146A>C	NP_001171504.1:p.Lys49Thr
NM_001243804.1:c.77A>C	NP_001230733.1:p.Lys26Thr
NM_018684.3:c.146A>C	NP_061154.1:p.Lys49Thr
NR_045044.1:n.557A>C
NM_018684.4:c.146A>C MANE Select	NP_061154.1:p.Lys49Thr
NM_001178032.3:c.77A>C	NP_001171503.1:p.Lys26Thr
NM_001243804.2:c.77A>C	NP_001230733.1:p.Lys26Thr
NR_045044.2:n.474A>C
NM_001178033.3:c.146A>C	NP_001171504.1:p.Lys49Thr