Canonical Allele Identifier: CA2663032737

Gene: SMARCAL1

Linked Data

• gnomAD v4: 2-216415538-G-GTTTTTTTTTTTTTTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216415553_216415554insTTTTTTTTTTTTTTTTTTTTTTTTT , CM000664.2:g.216415553_216415554insTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000002.11:g.217280276_217280277insTTTTTTTTTTTTTTTTTTTTTTTTT , CM000664.1:g.217280276_217280277insTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000002.10:g.216988521_216988522insTTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_009771.1:g.8140_8141insTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_108:g.8140_8141insTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000394410.2:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000430374.6:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000405077.2:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000444508.6:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000398969.2:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000697898.1:n.1172+38_1172+39insTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000697899.1:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000513470.1:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000697900.1:n.1087+38_1087+39insTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000697901.1:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000513471.1:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000697902.1:n.1043+38_1043+39insTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000697903.1:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000513472.1:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000697904.1:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000513473.1:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000697905.1:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000513474.1:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000697906.1:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000513475.1:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000697907.1:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000513476.1:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000357276.9:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000349823.4:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000357276.8:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000349823.4:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000358207.9:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000350940.5:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000392128.6:c.403+38_403+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000375974.2:n.403+38_403+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000427645.5:c.508+38_508+39insTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000392997.1:n.508+38_508+39insTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_001127207.1:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001120679.1:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_014140.3:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_108t1:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	NP_054859.2:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT
XM_005246631.2:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005246688.1:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT
XM_005246632.1:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005246689.1:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT
XM_006712557.1:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006712620.1:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT
XM_005246632.2:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005246689.1:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT
XM_017004228.2:c.-106+38_-106+39insTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016859717.1:n.-106+38_-106+39insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001127207.2:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001120679.1:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_014140.4:c.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_054859.2:n.811+38_811+39insTTTTTTTTTTTTTTTTTTTTTTTTT