Canonical Allele Identifier: CA103070461

Gene: BANK1

Linked Data

• dbSNP Id: rs969768211
• gnomAD v2: 4-102839041-TCTG-T
• gnomAD v3: 4-101917884-TCTG-T
• gnomAD v4: 4-101917884-TCTG-T
• MyVariant Identifiers: chr4:g.102839042_102839044del (hg19) ; chr4:g.101917885_101917887del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101917888_101917890del , CM000666.2:g.101917888_101917890del	GRCh38
NC_000004.11:g.102839045_102839047del , CM000666.1:g.102839045_102839047del	GRCh37
NC_000004.10:g.103058068_103058070del	NCBI36
NG_015824.1:g.132282_132284del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1010-105_1010-103del MANE Select	ENSP00000320509.4:n.1010-105_1010-103del
ENST00000322953.8:c.1010-105_1010-103del	ENSP00000320509.4:n.1010-105_1010-103del
ENST00000428908.5:c.611-105_611-103del	ENSP00000412748.1:n.611-105_611-103del
ENST00000444316.2:c.920-105_920-103del	ENSP00000388817.2:n.920-105_920-103del
ENST00000504592.5:c.965-105_965-103del	ENSP00000421443.1:n.965-105_965-103del
ENST00000508653.5:c.611-105_611-103del	ENSP00000422314.1:n.611-105_611-103del
NM_001083907.2:c.920-105_920-103del	NP_001077376.2:n.920-105_920-103del
NM_001127507.2:c.611-105_611-103del	NP_001120979.2:n.611-105_611-103del
NM_017935.4:c.1010-105_1010-103del	NP_060405.4:n.1010-105_1010-103del
XM_017008337.2:c.920-105_920-103del	XP_016863826.1:n.920-105_920-103del
NM_017935.5:c.1010-105_1010-103del MANE Select	NP_060405.5:n.1010-105_1010-103del
NM_001083907.3:c.920-105_920-103del	NP_001077376.3:n.920-105_920-103del
NM_001127507.3:c.611-105_611-103del	NP_001120979.3:n.611-105_611-103del