Canonical Allele Identifier: CA1024496057

Gene: SMARCB1

Linked Data

• gnomAD v3: 22-23793798-T-TTTTG
• gnomAD v4: 22-23793798-T-TTTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23793798_23793799insTTTG , CM000684.2:g.23793798_23793799insTTTG	GRCh38
NC_000022.10:g.24135985_24135986insTTTG , CM000684.1:g.24135985_24135986insTTTG	GRCh37
NC_000022.9:g.22465985_22465986insTTTG	NCBI36
NG_009303.1:g.11836_11837insTTTG , LRG_520:g.11836_11837insTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263121.12:c.362+110_362+111insTTTG	ENSP00000263121.8:n.362+110_362+111insTTTG
ENST00000344921.11:c.335+110_335+111insTTTG	ENSP00000340883.6:n.335+110_335+111insTTTG
ENST00000407082.4:c.335+110_335+111insTTTG	ENSP00000385226.4:n.335+110_335+111insTTTG
ENST00000407422.8:c.335+110_335+111insTTTG	ENSP00000383984.3:n.335+110_335+111insTTTG
ENST00000417137.6:c.362+110_362+111insTTTG	ENSP00000388489.2:n.362+110_362+111insTTTG
ENST00000491967.2:n.525+110_525+111insTTTG
ENST00000643421.1:n.330+110_330+111insTTTG
ENST00000644036.2:c.362+110_362+111insTTTG MANE Select	ENSP00000494049.2:n.362+110_362+111insTTTG
ENST00000644462.1:c.197+110_197+111insTTTG	ENSP00000494283.1:n.197+110_197+111insTTTG
ENST00000644619.1:c.362+110_362+111insTTTG	ENSP00000494695.1:n.362+110_362+111insTTTG
ENST00000646421.1:n.2218+110_2218+111insTTTG
ENST00000646723.1:n.350+110_350+111insTTTG
ENST00000646911.1:n.274+110_274+111insTTTG
ENST00000647057.1:c.93+6536_93+6537insTTTG	ENSP00000494757.1:n.93+6536_93+6537insTTTG
ENST00000263121.11:c.362+110_362+111insTTTG	ENSP00000263121.7:n.362+110_362+111insTTTG
ENST00000344921.10:c.335+110_335+111insTTTG	ENSP00000340883.6:n.335+110_335+111insTTTG
ENST00000407082.3:c.362+110_362+111insTTTG	ENSP00000385226.3:n.362+110_362+111insTTTG
ENST00000407422.7:c.335+110_335+111insTTTG	ENSP00000383984.3:n.335+110_335+111insTTTG
ENST00000417137.5:c.362+110_362+111insTTTG	ENSP00000388489.1:n.362+110_362+111insTTTG
ENST00000491967.1:n.88+110_88+111insTTTG
ENST00000634926.1:c.214+110_214+111insTTTG
ENST00000635578.1:c.187+110_187+111insTTTG
NM_001007468.1:c.335+110_335+111insTTTG	NP_001007469.1:n.335+110_335+111insTTTG
NM_003073.3:c.362+110_362+111insTTTG , LRG_520t1:c.362+110_362+111insTTTG	NP_003064.2:n.362+110_362+111insTTTG
XM_011530345.1:c.362+110_362+111insTTTG	XP_011528647.1:n.362+110_362+111insTTTG
XM_011530346.1:c.335+110_335+111insTTTG	XP_011528648.1:n.335+110_335+111insTTTG
NM_001007468.2:c.335+110_335+111insTTTG	NP_001007469.1:n.335+110_335+111insTTTG
NM_001317946.1:c.335+110_335+111insTTTG	NP_001304875.1:n.335+110_335+111insTTTG
NM_001362877.1:c.362+110_362+111insTTTG	NP_001349806.1:n.362+110_362+111insTTTG
NM_003073.4:c.362+110_362+111insTTTG	NP_003064.2:n.362+110_362+111insTTTG
NM_001007468.3:c.335+110_335+111insTTTG	NP_001007469.1:n.335+110_335+111insTTTG
NM_001317946.2:c.335+110_335+111insTTTG	NP_001304875.1:n.335+110_335+111insTTTG
NM_001362877.2:c.362+110_362+111insTTTG	NP_001349806.1:n.362+110_362+111insTTTG
NM_003073.5:c.362+110_362+111insTTTG MANE Select	NP_003064.2:n.362+110_362+111insTTTG