Canonical Allele Identifier: CA1481089994

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818498_101818501delinsTTGA , CM000666.2:g.101818498_101818501delinsTTGA	GRCh38
NC_000004.11:g.102739655_102739658delinsTTGA , CM000666.1:g.102739655_102739658delinsTTGA	GRCh37
NC_000004.10:g.102958678_102958681delinsTTGA	NCBI36
NG_015824.1:g.32892_32895delinsTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-11310_71-11307delinsTTGA MANE Select	ENSP00000320509.4:n.71-11310_71-11307delinsTTGA
ENST00000322953.8:c.71-11310_71-11307delinsTTGA	ENSP00000320509.4:n.71-11310_71-11307delinsTTGA
ENST00000428908.5:c.70+27548_70+27551delinsTTGA	ENSP00000412748.1:n.70+27548_70+27551delinsTTGA
ENST00000444316.2:c.-21+4560_-21+4563delinsTTGA	ENSP00000388817.2:n.-21+4560_-21+4563delinsTTGA
ENST00000504592.5:c.26-11310_26-11307delinsTTGA	ENSP00000421443.1:n.26-11310_26-11307delinsTTGA
ENST00000508653.5:c.70+27548_70+27551delinsTTGA	ENSP00000422314.1:n.70+27548_70+27551delinsTTGA
NM_001083907.2:c.-21+4560_-21+4563delinsTTGA	NP_001077376.2:n.-21+4560_-21+4563delinsTTGA
NM_001127507.2:c.70+27548_70+27551delinsTTGA	NP_001120979.2:n.70+27548_70+27551delinsTTGA
NM_017935.4:c.71-11310_71-11307delinsTTGA	NP_060405.4:n.71-11310_71-11307delinsTTGA
XM_017008337.2:c.-20-11310_-20-11307delinsTTGA	XP_016863826.1:n.-20-11310_-20-11307delinsTTGA
NM_017935.5:c.71-11310_71-11307delinsTTGA MANE Select	NP_060405.5:n.71-11310_71-11307delinsTTGA
NM_001083907.3:c.-21+4560_-21+4563delinsTTGA	NP_001077376.3:n.-21+4560_-21+4563delinsTTGA
NM_001127507.3:c.70+27548_70+27551delinsTTGA	NP_001120979.3:n.70+27548_70+27551delinsTTGA