Canonical Allele Identifier: CA357951758

Gene: BANK1

Linked Data

• MyVariant Identifiers: chr4:g.102750976G>C (hg19) ; chr4:g.101829819G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829819G>C , CM000666.2:g.101829819G>C	GRCh38
NC_000004.11:g.102750976G>C , CM000666.1:g.102750976G>C	GRCh37
NC_000004.10:g.102969999G>C	NCBI36
NG_015824.1:g.44213G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.82G>C MANE Select	ENSP00000320509.4:p.Asp28His
ENST00000322953.8:c.82G>C	ENSP00000320509.4:p.Asp28His
ENST00000428908.5:c.71-25216G>C	ENSP00000412748.1:n.71-25216G>C
ENST00000444316.2:c.-9G>C	ENSP00000388817.2:n.-9G>C
ENST00000504592.5:c.37G>C	ENSP00000421443.1:p.Asp13His
ENST00000508653.5:c.71-25216G>C	ENSP00000422314.1:n.71-25216G>C
NM_001083907.2:c.-9G>C	NP_001077376.2:n.-9G>C
NM_001127507.2:c.71-25216G>C	NP_001120979.2:n.71-25216G>C
NM_017935.4:c.82G>C	NP_060405.4:p.Asp28His
XM_017008337.2:c.-9G>C	XP_016863826.1:n.-9G>C
NM_017935.5:c.82G>C MANE Select	NP_060405.5:p.Asp28His
NM_001083907.3:c.-9G>C	NP_001077376.3:n.-9G>C
NM_001127507.3:c.71-25216G>C	NP_001120979.3:n.71-25216G>C