Canonical Allele Identifier: CA356651558

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39278647G>C (hg19) ; chr4:g.39277027G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277027G>C , CM000666.2:g.39277027G>C	GRCh38
NC_000004.11:g.39278647G>C , CM000666.1:g.39278647G>C	GRCh37
NC_000004.10:g.38955042G>C	NCBI36
NG_031813.1:g.99624G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3724G>C MANE Select	ENSP00000382717.3:p.Asp1242His
ENST00000399820.7:c.3724G>C	ENSP00000382717.3:p.Asp1242His
ENST00000503733.1:n.64G>C
ENST00000506869.5:c.*3305G>C	ENSP00000424319.1:n.*3305G>C
ENST00000512534.5:n.2035G>C
ENST00000512588.5:n.66G>C
NM_025132.3:c.3724G>C	NP_079408.3:p.Asp1242His
XM_011513724.1:c.3736G>C	XP_011512026.1:p.Asp1246His
XM_011513725.1:c.3670G>C	XP_011512027.1:p.Asp1224His
XM_011513726.1:c.3256G>C	XP_011512028.1:p.Asp1086His
XM_011513727.1:c.3256G>C	XP_011512029.1:p.Asp1086His
XM_011513728.1:c.3244G>C	XP_011512030.1:p.Asp1082His
XR_925155.1:n.5434G>C
NM_001317924.1:c.3244G>C	NP_001304853.1:p.Asp1082His
XM_011513725.2:c.3670G>C	XP_011512027.1:p.Asp1224His
XM_011513726.3:c.3256G>C	XP_011512028.1:p.Asp1086His
XM_017008501.1:c.3244G>C	XP_016863990.1:p.Asp1082His
XR_001741306.1:n.4001G>C
XR_001741307.1:n.3989G>C
XR_001741308.1:n.5635G>C
XR_001741309.1:n.5422G>C
XR_001741310.1:n.5623G>C
XR_001741311.2:n.5271G>C
NM_025132.4:c.3724G>C MANE Select	NP_079408.3:p.Asp1242His
NM_001317924.2:c.3244G>C	NP_001304853.1:p.Asp1082His