Canonical Allele Identifier: CA405452747

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593873G>C (hg19) ; chr19:g.36102971G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102971G>C , CM000681.2:g.36102971G>C	GRCh38
NC_000019.9:g.36593873G>C , CM000681.1:g.36593873G>C	GRCh37
NC_000019.8:g.41285713G>C	NCBI36
NG_028101.1:g.53091G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3344G>C	ENSP00000270301.6:p.Arg1115Pro
ENST00000401500.7:c.3359G>C MANE Select	ENSP00000384792.1:p.Arg1120Pro
ENST00000587391.6:c.*3219G>C	ENSP00000465525.1:n.*3219G>C
ENST00000679357.1:c.1439G>C
ENST00000679598.1:c.124G>C
ENST00000679682.1:c.3344G>C	ENSP00000506226.1:p.Arg1115Pro
ENST00000679714.1:c.3353G>C	ENSP00000506627.1:p.Arg1118Pro
ENST00000679757.1:c.3008G>C	ENSP00000505158.1:p.Arg1003Pro
ENST00000679858.1:c.*2741G>C	ENSP00000505655.1:n.*2741G>C
ENST00000680211.1:c.-41G>C	ENSP00000506102.1:n.-41G>C
ENST00000680280.1:n.646G>C
ENST00000680349.1:n.1927G>C
ENST00000680403.1:c.3344G>C	ENSP00000505677.1:p.Arg1115Pro
ENST00000680564.1:c.3110G>C	ENSP00000505582.1:p.Arg1037Pro
ENST00000680590.1:c.*1739G>C	ENSP00000505350.1:n.*1739G>C
ENST00000680597.1:c.124G>C
ENST00000680739.1:c.374G>C
ENST00000680773.1:n.1860G>C
ENST00000680806.1:c.*2662G>C	ENSP00000506418.1:n.*2662G>C
ENST00000680997.1:n.1291G>C
ENST00000681608.1:n.988G>C
ENST00000681625.1:c.*691G>C	ENSP00000505555.1:n.*691G>C
ENST00000681648.1:n.658G>C
ENST00000270301.11:c.3344G>C	ENSP00000270301.6:p.Arg1115Pro
ENST00000401500.6:c.3359G>C	ENSP00000384792.1:p.Arg1120Pro
ENST00000587391.5:c.*3219G>C	ENSP00000465525.1:n.*3219G>C
NM_001083961.1:c.3359G>C	NP_001077430.1:p.Arg1120Pro
NM_173636.4:c.3344G>C	NP_775907.4:p.Arg1115Pro
XM_005258809.2:c.3248G>C	XP_005258866.1:p.Arg1083Pro
XM_011526837.1:c.3344G>C	XP_011525139.1:p.Arg1115Pro
XM_011526838.1:c.3110G>C	XP_011525140.1:p.Arg1037Pro
XM_011526839.1:c.3008G>C	XP_011525141.1:p.Arg1003Pro
XM_011526840.1:c.2351G>C	XP_011525142.1:p.Arg784Pro
XM_011526841.1:c.1937G>C	XP_011525143.1:p.Arg646Pro
XM_011526842.1:c.1790G>C	XP_011525144.1:p.Arg597Pro
XM_011526843.1:c.1106G>C	XP_011525145.1:p.Arg369Pro
XM_011526844.1:c.1106G>C	XP_011525146.1:p.Arg369Pro
XM_011526840.2:c.2351G>C	XP_011525142.1:p.Arg784Pro
XM_011526841.2:c.1937G>C	XP_011525143.1:p.Arg646Pro
XM_011526844.2:c.1106G>C	XP_011525146.1:p.Arg369Pro
XM_017026665.1:c.3359G>C	XP_016882154.1:p.Arg1120Pro
NM_001083961.2:c.3359G>C MANE Select	NP_001077430.1:p.Arg1120Pro
NM_173636.5:c.3344G>C	NP_775907.4:p.Arg1115Pro