Canonical Allele Identifier: CA3054209141

Gene: RECQL4

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144515245_144515246delinsAA , CM000670.2:g.144515245_144515246delinsAA	GRCh38
NC_000008.10:g.145740629_145740630delinsAA , CM000670.1:g.145740629_145740630delinsAA	GRCh37
NC_000008.9:g.145711437_145711438delinsAA	NCBI36
NG_016430.1:g.7581_7582delinsTT
NG_033083.1:g.2281_2282delinsAA
NG_016430.2:g.7581_7582delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688394.1:n.414-4_414-3delinsTT
ENST00000617875.6:c.1391-4_1391-3delinsTT MANE Select	ENSP00000482313.2:n.1391-4_1391-3delinsTT
ENST00000532846.2:c.276-4_276-3delinsTT
ENST00000617875.4:c.1391-4_1391-3delinsTT	ENSP00000482313.1:n.1391-4_1391-3delinsTT
ENST00000621189.4:c.320-4_320-3delinsTT	ENSP00000483145.1:n.320-4_320-3delinsTT
NM_004260.3:c.1391-4_1391-3delinsTT	NP_004251.3:n.1391-4_1391-3delinsTT
XM_011517380.1:c.1391-4_1391-3delinsTT	XP_011515682.1:n.1391-4_1391-3delinsTT
XM_011517381.1:c.1295-4_1295-3delinsTT	XP_011515683.1:n.1295-4_1295-3delinsTT
XM_011517382.1:c.1391-4_1391-3delinsTT	XP_011515684.1:n.1391-4_1391-3delinsTT
XM_011517383.1:c.1391-4_1391-3delinsTT	XP_011515685.1:n.1391-4_1391-3delinsTT
XM_011517384.1:c.1391-4_1391-3delinsTT	XP_011515686.1:n.1391-4_1391-3delinsTT
XM_011517385.1:c.254-4_254-3delinsTT	XP_011515687.1:n.254-4_254-3delinsTT
XR_928366.1:n.1432-4_1432-3delinsTT
XR_928367.1:n.1432-4_1432-3delinsTT
XR_928368.1:n.1434-4_1434-3delinsTT
XM_011517384.3:c.1391-4_1391-3delinsTT	XP_011515686.1:n.1391-4_1391-3delinsTT
XM_017013991.2:c.1391-4_1391-3delinsTT	XP_016869480.1:n.1391-4_1391-3delinsTT
XM_017013992.2:c.1391-4_1391-3delinsTT	XP_016869481.1:n.1391-4_1391-3delinsTT
XM_017013993.2:c.1391-4_1391-3delinsTT	XP_016869482.1:n.1391-4_1391-3delinsTT
XM_017013994.2:c.1295-4_1295-3delinsTT	XP_016869483.1:n.1295-4_1295-3delinsTT
XM_017013995.2:c.1391-4_1391-3delinsTT	XP_016869484.1:n.1391-4_1391-3delinsTT
XM_017013996.2:c.1391-4_1391-3delinsTT	XP_016869485.1:n.1391-4_1391-3delinsTT
XM_017013997.2:c.1391-4_1391-3delinsTT	XP_016869486.1:n.1391-4_1391-3delinsTT
XM_017013998.1:c.1391-4_1391-3delinsTT	XP_016869487.1:n.1391-4_1391-3delinsTT
XM_017013999.2:c.1391-4_1391-3delinsTT	XP_016869488.1:n.1391-4_1391-3delinsTT
XM_017014000.1:c.254-4_254-3delinsTT	XP_016869489.1:n.254-4_254-3delinsTT
XM_017014001.2:c.254-4_254-3delinsTT	XP_016869490.1:n.254-4_254-3delinsTT
XR_001745626.2:n.1428-4_1428-3delinsTT
XR_001745627.2:n.1428-4_1428-3delinsTT
XR_001745628.2:n.1428-4_1428-3delinsTT
XR_001745629.2:n.1428-4_1428-3delinsTT
XR_001745630.2:n.1428-4_1428-3delinsTT
NM_004260.4:c.1391-4_1391-3delinsTT MANE Select	NP_004251.4:n.1391-4_1391-3delinsTT