Canonical Allele Identifier: CA784480478

Gene: BANK1

Linked Data

• dbSNP Id: rs1201398221
• MyVariant Identifiers: chr4:g.102739656_102739658del (hg19) ; chr4:g.101818499_101818501del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818501_101818503del , CM000666.2:g.101818501_101818503del	GRCh38
NC_000004.11:g.102739658_102739660del , CM000666.1:g.102739658_102739660del	GRCh37
NC_000004.10:g.102958681_102958683del	NCBI36
NG_015824.1:g.32895_32897del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-11307_71-11305del MANE Select	ENSP00000320509.4:n.71-11307_71-11305del
ENST00000322953.8:c.71-11307_71-11305del	ENSP00000320509.4:n.71-11307_71-11305del
ENST00000428908.5:c.70+27551_70+27553del	ENSP00000412748.1:n.70+27551_70+27553del
ENST00000444316.2:c.-21+4563_-21+4565del	ENSP00000388817.2:n.-21+4563_-21+4565del
ENST00000504592.5:c.26-11307_26-11305del	ENSP00000421443.1:n.26-11307_26-11305del
ENST00000508653.5:c.70+27551_70+27553del	ENSP00000422314.1:n.70+27551_70+27553del
NM_001083907.2:c.-21+4563_-21+4565del	NP_001077376.2:n.-21+4563_-21+4565del
NM_001127507.2:c.70+27551_70+27553del	NP_001120979.2:n.70+27551_70+27553del
NM_017935.4:c.71-11307_71-11305del	NP_060405.4:n.71-11307_71-11305del
XM_017008337.2:c.-20-11307_-20-11305del	XP_016863826.1:n.-20-11307_-20-11305del
NM_017935.5:c.71-11307_71-11305del MANE Select	NP_060405.5:n.71-11307_71-11305del
NM_001083907.3:c.-21+4563_-21+4565del	NP_001077376.3:n.-21+4563_-21+4565del
NM_001127507.3:c.70+27551_70+27553del	NP_001120979.3:n.70+27551_70+27553del