Canonical Allele Identifier: CA2648141512
Gene: HAX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154275389G>A , CM000663.2:g.154275389G>A GRCh38
NC_000001.10:g.154247865G>A , CM000663.1:g.154247865G>A GRCh37
NC_000001.9:g.152514489G>A NCBI36
NG_007369.1:g.7827G>A , LRG_64:g.7827G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435087.2:c.676-4G>A ENSP00000394920.2:n.676-4G>A
ENST00000447768.7:c.*24-4G>A ENSP00000403848.2:n.*24-4G>A
ENST00000459914.2:n.917-4G>A
ENST00000471326.6:n.1340-4G>A
ENST00000483970.7:c.688-4G>A ENSP00000435088.1:n.688-4G>A
ENST00000531435.6:n.1009-4G>A
ENST00000696929.1:c.*155-4G>A ENSP00000512978.1:n.*155-4G>A
ENST00000696930.1:n.1337-4G>A
ENST00000696931.1:n.1045G>A
ENST00000696932.1:c.664-4G>A ENSP00000512979.1:n.664-4G>A
ENST00000696933.1:c.*24-4G>A ENSP00000512980.1:n.*24-4G>A
ENST00000696938.1:c.655-4G>A ENSP00000512983.1:n.655-4G>A
ENST00000696941.1:c.586-4G>A ENSP00000512986.1:n.586-4G>A
ENST00000696944.1:c.586-4G>A ENSP00000512989.1:n.586-4G>A
ENST00000697592.1:c.586-4G>A ENSP00000513356.1:n.586-4G>A
ENST00000697830.1:c.586-4G>A ENSP00000513452.1:n.586-4G>A
ENST00000328703.12:c.664-4G>A MANE Select ENSP00000329002.7:n.664-4G>A
ENST00000328703.11:c.664-4G>A ENSP00000329002.7:n.664-4G>A
ENST00000435087.1:c.676-4G>A ENSP00000394920.1:n.676-4G>A
ENST00000447768.6:c.*24-4G>A ENSP00000403848.2:n.*24-4G>A
ENST00000457918.6:c.520-4G>A ENSP00000411448.2:n.520-4G>A
ENST00000459914.1:n.376-4G>A
ENST00000471326.5:n.1079-4G>A
ENST00000483970.6:c.688-4G>A ENSP00000435088.1:n.688-4G>A
ENST00000492550.1:n.381G>A
ENST00000531435.5:n.934-4G>A
ENST00000532105.1:c.280-4G>A ENSP00000433951.1:n.280-4G>A
NM_001018837.1:c.520-4G>A NP_001018238.1:n.520-4G>A
NM_006118.3:c.664-4G>A , LRG_64t1:c.664-4G>A NP_006109.2:n.664-4G>A
NM_001018837.2:c.520-4G>A NP_001018238.1:n.520-4G>A
NM_006118.4:c.664-4G>A MANE Select NP_006109.2:n.664-4G>A