Canonical Allele Identifier: CA2671540439

Gene: BANK1

Linked Data

• gnomAD v4: 4-101829733-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829737del , CM000666.2:g.101829737del	GRCh38
NC_000004.11:g.102750894del , CM000666.1:g.102750894del	GRCh37
NC_000004.10:g.102969917del	NCBI36
NG_015824.1:g.44131del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-71del MANE Select	ENSP00000320509.4:n.71-71del
ENST00000322953.8:c.71-71del	ENSP00000320509.4:n.71-71del
ENST00000428908.5:c.71-25298del	ENSP00000412748.1:n.71-25298del
ENST00000444316.2:c.-20-71del	ENSP00000388817.2:n.-20-71del
ENST00000504592.5:c.26-71del	ENSP00000421443.1:n.26-71del
ENST00000508653.5:c.71-25298del	ENSP00000422314.1:n.71-25298del
NM_001083907.2:c.-20-71del	NP_001077376.2:n.-20-71del
NM_001127507.2:c.71-25298del	NP_001120979.2:n.71-25298del
NM_017935.4:c.71-71del	NP_060405.4:n.71-71del
XM_017008337.2:c.-20-71del	XP_016863826.1:n.-20-71del
NM_017935.5:c.71-71del MANE Select	NP_060405.5:n.71-71del
NM_001083907.3:c.-20-71del	NP_001077376.3:n.-20-71del
NM_001127507.3:c.71-25298del	NP_001120979.3:n.71-25298del