Canonical Allele Identifier: CA1481090195

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818890_101818891delinsTA , CM000666.2:g.101818890_101818891delinsTA	GRCh38
NC_000004.11:g.102740047_102740048delinsTA , CM000666.1:g.102740047_102740048delinsTA	GRCh37
NC_000004.10:g.102959070_102959071delinsTA	NCBI36
NG_015824.1:g.33284_33285delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-10918_71-10917delinsTA MANE Select	ENSP00000320509.4:n.71-10918_71-10917delinsTA
ENST00000322953.8:c.71-10918_71-10917delinsTA	ENSP00000320509.4:n.71-10918_71-10917delinsTA
ENST00000428908.5:c.70+27940_70+27941delinsTA	ENSP00000412748.1:n.70+27940_70+27941delinsTA
ENST00000444316.2:c.-21+4952_-21+4953delinsTA	ENSP00000388817.2:n.-21+4952_-21+4953delinsTA
ENST00000504592.5:c.26-10918_26-10917delinsTA	ENSP00000421443.1:n.26-10918_26-10917delinsTA
ENST00000508653.5:c.70+27940_70+27941delinsTA	ENSP00000422314.1:n.70+27940_70+27941delinsTA
NM_001083907.2:c.-21+4952_-21+4953delinsTA	NP_001077376.2:n.-21+4952_-21+4953delinsTA
NM_001127507.2:c.70+27940_70+27941delinsTA	NP_001120979.2:n.70+27940_70+27941delinsTA
NM_017935.4:c.71-10918_71-10917delinsTA	NP_060405.4:n.71-10918_71-10917delinsTA
XM_017008337.2:c.-20-10918_-20-10917delinsTA	XP_016863826.1:n.-20-10918_-20-10917delinsTA
NM_017935.5:c.71-10918_71-10917delinsTA MANE Select	NP_060405.5:n.71-10918_71-10917delinsTA
NM_001083907.3:c.-21+4952_-21+4953delinsTA	NP_001077376.3:n.-21+4952_-21+4953delinsTA
NM_001127507.3:c.70+27940_70+27941delinsTA	NP_001120979.3:n.70+27940_70+27941delinsTA