Canonical Allele Identifier: CA553724841

Gene: BANK1

Linked Data

• dbSNP Id: rs1379885412
• gnomAD v2: 4-102750739-TTATAC-T
• gnomAD v3: 4-101829582-TTATAC-T
• gnomAD v4: 4-101829582-TTATAC-T
• MyVariant Identifiers: chr4:g.102750740_102750744del (hg19) ; chr4:g.101829583_101829587del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829584_101829588del , CM000666.2:g.101829584_101829588del	GRCh38
NC_000004.11:g.102750741_102750745del , CM000666.1:g.102750741_102750745del	GRCh37
NC_000004.10:g.102969764_102969768del	NCBI36
NG_015824.1:g.43978_43982del

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.71-224_71-220del MANE Select	ENSP00000320509.4:n.71-224_71-220del
ENST00000322953.8:c.71-224_71-220del	ENSP00000320509.4:n.71-224_71-220del
ENST00000428908.5:c.71-25451_71-25447del	ENSP00000412748.1:n.71-25451_71-25447del
ENST00000444316.2:c.-20-224_-20-220del	ENSP00000388817.2:n.-20-224_-20-220del
ENST00000504592.5:c.26-224_26-220del	ENSP00000421443.1:n.26-224_26-220del
ENST00000508653.5:c.71-25451_71-25447del	ENSP00000422314.1:n.71-25451_71-25447del
NM_001083907.2:c.-20-224_-20-220del	NP_001077376.2:n.-20-224_-20-220del
NM_001127507.2:c.71-25451_71-25447del	NP_001120979.2:n.71-25451_71-25447del
NM_017935.4:c.71-224_71-220del	NP_060405.4:n.71-224_71-220del
XM_017008337.2:c.-20-224_-20-220del	XP_016863826.1:n.-20-224_-20-220del
NM_017935.5:c.71-224_71-220del MANE Select	NP_060405.5:n.71-224_71-220del
NM_001083907.3:c.-20-224_-20-220del	NP_001077376.3:n.-20-224_-20-220del
NM_001127507.3:c.71-25451_71-25447del	NP_001120979.3:n.71-25451_71-25447del