Canonical Allele Identifier: CA1066075892

Gene: BANK1

Linked Data

• gnomAD v3: 4-101818892-G-GTTT
• gnomAD v4: 4-101818892-G-GTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818893_101818895dup , CM000666.2:g.101818893_101818895dup	GRCh38
NC_000004.11:g.102740050_102740052dup , CM000666.1:g.102740050_102740052dup	GRCh37
NC_000004.10:g.102959073_102959075dup	NCBI36
NG_015824.1:g.33287_33289dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-10915_71-10913dup MANE Select	ENSP00000320509.4:n.71-10915_71-10913dup
ENST00000322953.8:c.71-10915_71-10913dup	ENSP00000320509.4:n.71-10915_71-10913dup
ENST00000428908.5:c.70+27943_70+27945dup	ENSP00000412748.1:n.70+27943_70+27945dup
ENST00000444316.2:c.-21+4955_-21+4957dup	ENSP00000388817.2:n.-21+4955_-21+4957dup
ENST00000504592.5:c.26-10915_26-10913dup	ENSP00000421443.1:n.26-10915_26-10913dup
ENST00000508653.5:c.70+27943_70+27945dup	ENSP00000422314.1:n.70+27943_70+27945dup
NM_001083907.2:c.-21+4955_-21+4957dup	NP_001077376.2:n.-21+4955_-21+4957dup
NM_001127507.2:c.70+27943_70+27945dup	NP_001120979.2:n.70+27943_70+27945dup
NM_017935.4:c.71-10915_71-10913dup	NP_060405.4:n.71-10915_71-10913dup
XM_017008337.2:c.-20-10915_-20-10913dup	XP_016863826.1:n.-20-10915_-20-10913dup
NM_017935.5:c.71-10915_71-10913dup MANE Select	NP_060405.5:n.71-10915_71-10913dup
NM_001083907.3:c.-21+4955_-21+4957dup	NP_001077376.3:n.-21+4955_-21+4957dup
NM_001127507.3:c.70+27943_70+27945dup	NP_001120979.3:n.70+27943_70+27945dup