Canonical Allele Identifier: CA356634206

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39233575A>C (hg19) ; chr4:g.39231955A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39231955A>C , CM000666.2:g.39231955A>C	GRCh38
NC_000004.11:g.39233575A>C , CM000666.1:g.39233575A>C	GRCh37
NC_000004.10:g.38909970A>C	NCBI36
NG_031813.1:g.54552A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.2141A>C MANE Select	ENSP00000382717.3:p.Lys714Thr
ENST00000399820.7:c.2141A>C	ENSP00000382717.3:p.Lys714Thr
ENST00000506869.5:c.*1722A>C	ENSP00000424319.1:n.*1722A>C
ENST00000507228.1:c.319A>C
ENST00000511729.5:n.332A>C
ENST00000512095.5:n.1139A>C
ENST00000515631.1:n.295A>C
NM_025132.3:c.2141A>C	NP_079408.3:p.Lys714Thr
XM_011513724.1:c.2141A>C	XP_011512026.1:p.Lys714Thr
XM_011513725.1:c.2075A>C	XP_011512027.1:p.Lys692Thr
XM_011513726.1:c.1661A>C	XP_011512028.1:p.Lys554Thr
XM_011513727.1:c.1661A>C	XP_011512029.1:p.Lys554Thr
XM_011513728.1:c.1661A>C	XP_011512030.1:p.Lys554Thr
XM_011513729.1:c.2141A>C	XP_011512031.1:p.Lys714Thr
XR_925155.1:n.2205A>C
NM_001317924.1:c.1661A>C	NP_001304853.1:p.Lys554Thr
XM_011513725.2:c.2075A>C	XP_011512027.1:p.Lys692Thr
XM_011513726.3:c.1661A>C	XP_011512028.1:p.Lys554Thr
XM_017008501.1:c.1661A>C	XP_016863990.1:p.Lys554Thr
XR_001741306.1:n.2205A>C
XR_001741307.1:n.2205A>C
XR_001741308.1:n.2205A>C
XR_001741309.1:n.2205A>C
XR_001741310.1:n.2205A>C
XR_001741311.2:n.2054A>C
XR_001741312.1:n.2205A>C
NM_025132.4:c.2141A>C MANE Select	NP_079408.3:p.Lys714Thr
NM_001317924.2:c.1661A>C	NP_001304853.1:p.Lys554Thr