Canonical Allele Identifier: CA409718698

Gene: DNAJC5

Linked Data

• COSMIC: COSM5672805 ; COSM5672806
• MyVariant Identifiers: chr20:g.62562247G>T (hg19) ; chr20:g.63930894G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63930894G>T , CM000682.2:g.63930894G>T	GRCh38
NC_000020.10:g.62562247G>T , CM000682.1:g.62562247G>T	GRCh37
NC_000020.9:g.62032691G>T	NCBI36
NG_029805.1:g.40793G>T
NG_029805.2:g.40793G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703637.1:c.365G>T	ENSP00000515413.1:p.Cys122Phe
ENST00000360864.9:c.365G>T MANE Select	ENSP00000354111.4:p.Cys122Phe
ENST00000360864.8:c.365G>T	ENSP00000354111.4:p.Cys122Phe
ENST00000470551.1:c.365G>T	ENSP00000434744.1:p.Cys122Phe
NM_025219.2:c.365G>T	NP_079495.1:p.Cys122Phe
XM_011529048.1:c.365G>T	XP_011527350.1:p.Cys122Phe
XM_011529049.1:c.365G>T	XP_011527351.1:p.Cys122Phe
XM_011529050.1:c.365G>T	XP_011527352.1:p.Cys122Phe
XR_936629.1:n.997G>T
XR_936630.1:n.1255G>T
XM_011529048.2:c.365G>T	XP_011527350.1:p.Cys122Phe
XR_936629.2:n.1010G>T
NM_025219.3:c.365G>T MANE Select	NP_079495.1:p.Cys122Phe