Canonical Allele Identifier: CA1826365418

Gene: RECQL4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144511868G= , CM000670.2:g.144511868G=	GRCh38
NC_000008.10:g.145737251G= , CM000670.1:g.145737251G=	GRCh37
NC_000008.9:g.145708059G=	NCBI36
NG_016430.1:g.10959C=
NG_016430.2:g.10959C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617875.6:c.3393+43C= MANE Select	ENSP00000482313.2:n.3393+43C=
ENST00000301323.7:c.410+43C=
ENST00000529424.2:n.50-79C=
ENST00000531875.2:c.648+34C=	ENSP00000477910.1:n.648+34C=
ENST00000617875.4:c.3393+43C=	ENSP00000482313.1:n.3393+43C=
ENST00000621189.4:c.2322+43C=	ENSP00000483145.1:n.2322+43C=
NM_004260.3:c.3393+43C=	NP_004251.3:n.3393+43C=
XM_011517380.1:c.3468+43C=	XP_011515682.1:n.3468+43C=
XM_011517381.1:c.3372+43C=	XP_011515683.1:n.3372+43C=
XM_011517382.1:c.3276+43C=	XP_011515684.1:n.3276+43C=
XM_011517383.1:c.3270+43C=	XP_011515685.1:n.3270+43C=
XM_011517384.1:c.3195+43C=	XP_011515686.1:n.3195+43C=
XM_011517385.1:c.2331+43C=	XP_011515687.1:n.2331+43C=
XR_928366.1:n.3353-79C=
XR_928367.1:n.3448+43C=
XR_928368.1:n.3341+43C=
XM_011517384.3:c.3195+43C=	XP_011515686.1:n.3195+43C=
XM_017013991.2:c.3601C=	XP_016869480.1:p.Pro1201=
XM_017013992.2:c.3526C=	XP_016869481.1:p.Pro1176=
XM_017013993.2:c.3511C=	XP_016869482.1:p.Pro1171=
XM_017013994.2:c.3505C=	XP_016869483.1:p.Pro1169=
XM_017013995.2:c.3436C=	XP_016869484.1:p.Pro1146=
XM_017013996.2:c.3558+43C=	XP_016869485.1:n.3558+43C=
XM_017013997.2:c.3403C=	XP_016869486.1:p.Pro1135=
XM_017013998.1:c.3483+43C=	XP_016869487.1:n.3483+43C=
XM_017013999.2:c.3313C=	XP_016869488.1:p.Pro1105=
XM_017014000.1:c.2464C=	XP_016869489.1:p.Pro822=
XM_017014001.2:c.2374C=	XP_016869490.1:p.Pro792=
XR_001745626.2:n.3439-79C=
XR_001745627.2:n.3534+43C=
XR_001745628.2:n.3425+43C=
XR_001745629.2:n.3288+43C=
XR_001745630.2:n.3090+43C=
NM_004260.4:c.3393+43C= MANE Select	NP_004251.4:n.3393+43C=