Canonical Allele Identifier: CA1481088850

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101815936_101815937delinsTG , CM000666.2:g.101815936_101815937delinsTG	GRCh38
NC_000004.11:g.102737093_102737094delinsTG , CM000666.1:g.102737093_102737094delinsTG	GRCh37
NC_000004.10:g.102956116_102956117delinsTG	NCBI36
NG_015824.1:g.30330_30331delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-13872_71-13871delinsTG MANE Select	ENSP00000320509.4:n.71-13872_71-13871delinsTG
ENST00000322953.8:c.71-13872_71-13871delinsTG	ENSP00000320509.4:n.71-13872_71-13871delinsTG
ENST00000428908.5:c.70+24986_70+24987delinsTG	ENSP00000412748.1:n.70+24986_70+24987delinsTG
ENST00000444316.2:c.-21+1998_-21+1999delinsTG	ENSP00000388817.2:n.-21+1998_-21+1999delinsTG
ENST00000504592.5:c.26-13872_26-13871delinsTG	ENSP00000421443.1:n.26-13872_26-13871delinsTG
ENST00000508653.5:c.70+24986_70+24987delinsTG	ENSP00000422314.1:n.70+24986_70+24987delinsTG
NM_001083907.2:c.-21+1998_-21+1999delinsTG	NP_001077376.2:n.-21+1998_-21+1999delinsTG
NM_001127507.2:c.70+24986_70+24987delinsTG	NP_001120979.2:n.70+24986_70+24987delinsTG
NM_017935.4:c.71-13872_71-13871delinsTG	NP_060405.4:n.71-13872_71-13871delinsTG
XM_017008337.2:c.-20-13872_-20-13871delinsTG	XP_016863826.1:n.-20-13872_-20-13871delinsTG
NM_017935.5:c.71-13872_71-13871delinsTG MANE Select	NP_060405.5:n.71-13872_71-13871delinsTG
NM_001083907.3:c.-21+1998_-21+1999delinsTG	NP_001077376.3:n.-21+1998_-21+1999delinsTG
NM_001127507.3:c.70+24986_70+24987delinsTG	NP_001120979.3:n.70+24986_70+24987delinsTG