Canonical Allele Identifier: CA1817263239

Gene: WASHC5

Linked Data

• dbSNP Id: rs1816444206

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125057498T>G , CM000670.2:g.125057498T>G	GRCh38
NC_000008.10:g.126069740T>G , CM000670.1:g.126069740T>G	GRCh37
NC_000008.9:g.126138922T>G	NCBI36
NG_012636.1:g.39322A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318410.12:c.1875+58A>C MANE Select	ENSP00000318016.7:n.1875+58A>C
ENST00000318410.11:c.1875+58A>C	ENSP00000318016.7:n.1875+58A>C
ENST00000517845.5:c.1431+58A>C	ENSP00000429676.1:n.1431+58A>C
NM_014846.3:c.1875+58A>C	NP_055661.3:n.1875+58A>C
XM_005251120.2:c.1431+58A>C	XP_005251177.1:n.1431+58A>C
XM_011517409.1:c.1875+58A>C	XP_011515711.1:n.1875+58A>C
XM_011517410.1:c.1875+58A>C	XP_011515712.1:n.1875+58A>C
NM_001330609.1:c.1431+58A>C	NP_001317538.1:n.1431+58A>C
XM_017014113.2:c.1875+58A>C	XP_016869602.1:n.1875+58A>C
NM_014846.4:c.1875+58A>C MANE Select	NP_055661.3:n.1875+58A>C
NM_001330609.2:c.1431+58A>C	NP_001317538.1:n.1431+58A>C