Canonical Allele Identifier: CA357956383
Gene: BANK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101918140C>A , CM000666.2:g.101918140C>A GRCh38
NC_000004.11:g.102839297C>A , CM000666.1:g.102839297C>A GRCh37
NC_000004.10:g.103058320C>A NCBI36
NG_015824.1:g.132534C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322953.9:c.1157C>A MANE Select ENSP00000320509.4:p.Ala386Asp
ENST00000322953.8:c.1157C>A ENSP00000320509.4:p.Ala386Asp
ENST00000428908.5:c.758C>A ENSP00000412748.1:p.Ala253Asp
ENST00000444316.2:c.1067C>A ENSP00000388817.2:p.Ala356Asp
ENST00000504592.5:c.1112C>A ENSP00000421443.1:p.Ala371Asp
ENST00000508653.5:c.758C>A ENSP00000422314.1:p.Ala253Asp
NM_001083907.2:c.1067C>A NP_001077376.2:p.Ala356Asp
NM_001127507.2:c.758C>A NP_001120979.2:p.Ala253Asp
NM_017935.4:c.1157C>A NP_060405.4:p.Ala386Asp
XM_017008337.2:c.1067C>A XP_016863826.1:p.Ala356Asp
NM_017935.5:c.1157C>A MANE Select NP_060405.5:p.Ala386Asp
NM_001083907.3:c.1067C>A NP_001077376.3:p.Ala356Asp
NM_001127507.3:c.758C>A NP_001120979.3:p.Ala253Asp