Canonical Allele Identifier: CA10607753

Gene: HAX1

Linked Data

• ClinVar Variation Id: 292703
• ClinVar RCV Id: RCV000273006
• dbSNP Id: rs761500862
• gnomAD v2: 1-154245895-G-C
• gnomAD v3: 1-154273419-G-C
• gnomAD v4: 1-154273419-G-C
• MyVariant Identifiers: chr1:g.154245895G>C (hg19) ; chr1:g.154273419G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154273419G>C , CM000663.2:g.154273419G>C	GRCh38
NC_000001.10:g.154245895G>C , CM000663.1:g.154245895G>C	GRCh37
NC_000001.9:g.152512519G>C	NCBI36
NG_007369.1:g.5857G>C , LRG_64:g.5857G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435087.2:c.137G>C	ENSP00000394920.2:p.Arg46Pro
ENST00000447768.7:c.137G>C	ENSP00000403848.2:p.Arg46Pro
ENST00000459914.2:n.238G>C
ENST00000471326.6:n.813G>C
ENST00000477780.3:n.224G>C
ENST00000483970.7:c.137G>C	ENSP00000435088.1:p.Arg46Pro
ENST00000531435.6:n.307G>C
ENST00000696929.1:c.137G>C	ENSP00000512978.1:p.Arg46Pro
ENST00000696931.1:n.238G>C
ENST00000696932.1:c.137G>C	ENSP00000512979.1:p.Arg46Pro
ENST00000696933.1:c.137G>C	ENSP00000512980.1:p.Arg46Pro
ENST00000696938.1:c.137G>C	ENSP00000512983.1:p.Arg46Pro
ENST00000696941.1:c.59G>C	ENSP00000512986.1:p.Arg20Pro
ENST00000696944.1:c.59G>C	ENSP00000512989.1:p.Arg20Pro
ENST00000696945.1:c.59G>C	ENSP00000512990.1:p.Arg20Pro
ENST00000696965.1:c.59G>C	ENSP00000513004.1:p.Arg20Pro
ENST00000696966.1:c.59G>C	ENSP00000513005.1:p.Arg20Pro
ENST00000697592.1:c.59G>C	ENSP00000513356.1:p.Arg20Pro
ENST00000697830.1:c.59G>C	ENSP00000513452.1:p.Arg20Pro
ENST00000328703.12:c.137G>C MANE Select	ENSP00000329002.7:p.Arg46Pro
ENST00000328703.11:c.137G>C	ENSP00000329002.7:p.Arg46Pro
ENST00000435087.1:c.137G>C	ENSP00000394920.1:p.Arg46Pro
ENST00000447768.6:c.137G>C	ENSP00000403848.2:p.Arg46Pro
ENST00000457918.6:c.54-61G>C	ENSP00000411448.2:n.54-61G>C
ENST00000471326.5:n.552G>C
ENST00000477780.2:n.224G>C
ENST00000483970.6:c.137G>C	ENSP00000435088.1:p.Arg46Pro
ENST00000531435.5:n.232G>C
ENST00000532105.1:c.-68-355G>C	ENSP00000433951.1:n.-68-355G>C
NM_001018837.1:c.54-61G>C	NP_001018238.1:n.54-61G>C
NM_006118.3:c.137G>C , LRG_64t1:c.137G>C	NP_006109.2:p.Arg46Pro
NM_001018837.2:c.54-61G>C	NP_001018238.1:n.54-61G>C
NM_006118.4:c.137G>C MANE Select	NP_006109.2:p.Arg46Pro