Canonical Allele Identifier: CA356651531

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39278642G>C (hg19) ; chr4:g.39277022G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277022G>C , CM000666.2:g.39277022G>C	GRCh38
NC_000004.11:g.39278642G>C , CM000666.1:g.39278642G>C	GRCh37
NC_000004.10:g.38955037G>C	NCBI36
NG_031813.1:g.99619G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3719G>C MANE Select	ENSP00000382717.3:p.Arg1240Thr
ENST00000399820.7:c.3719G>C	ENSP00000382717.3:p.Arg1240Thr
ENST00000503733.1:n.59G>C
ENST00000506869.5:c.*3300G>C	ENSP00000424319.1:n.*3300G>C
ENST00000512534.5:n.2030G>C
ENST00000512588.5:n.61G>C
NM_025132.3:c.3719G>C	NP_079408.3:p.Arg1240Thr
XM_011513724.1:c.3731G>C	XP_011512026.1:p.Arg1244Thr
XM_011513725.1:c.3665G>C	XP_011512027.1:p.Arg1222Thr
XM_011513726.1:c.3251G>C	XP_011512028.1:p.Arg1084Thr
XM_011513727.1:c.3251G>C	XP_011512029.1:p.Arg1084Thr
XM_011513728.1:c.3239G>C	XP_011512030.1:p.Arg1080Thr
XR_925155.1:n.5429G>C
NM_001317924.1:c.3239G>C	NP_001304853.1:p.Arg1080Thr
XM_011513725.2:c.3665G>C	XP_011512027.1:p.Arg1222Thr
XM_011513726.3:c.3251G>C	XP_011512028.1:p.Arg1084Thr
XM_017008501.1:c.3239G>C	XP_016863990.1:p.Arg1080Thr
XR_001741306.1:n.3996G>C
XR_001741307.1:n.3984G>C
XR_001741308.1:n.5630G>C
XR_001741309.1:n.5417G>C
XR_001741310.1:n.5618G>C
XR_001741311.2:n.5266G>C
NM_025132.4:c.3719G>C MANE Select	NP_079408.3:p.Arg1240Thr
NM_001317924.2:c.3239G>C	NP_001304853.1:p.Arg1080Thr