Canonical Allele Identifier: CA4874047

Gene: WASHC5

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125078737C>T , CM000670.2:g.125078737C>T	GRCh38
NC_000008.10:g.126090979C>T , CM000670.1:g.126090979C>T	GRCh37
NC_000008.9:g.126160161C>T	NCBI36
NG_012636.1:g.18083G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014846.4:c.711+1G>A MANE Select	NP_055661.3:n.711+1G>A
ENST00000318410.12:c.711+1G>A MANE Select	ENSP00000318016.7:n.711+1G>A
NM_001330609.1:c.267+1G>A	NP_001317538.1:n.267+1G>A
NM_001330609.2:c.267+1G>A	NP_001317538.1:n.267+1G>A
NM_014846.3:c.711+1G>A	NP_055661.3:n.711+1G>A
ENST00000318410.11:c.711+1G>A	ENSP00000318016.7:n.711+1G>A
ENST00000517845.5:c.267+1G>A	ENSP00000429676.1:n.267+1G>A
ENST00000523297.5:c.267+1G>A	ENSP00000427946.1:n.267+1G>A
XM_005251120.2:c.267+1G>A	XP_005251177.1:n.267+1G>A
XM_011517409.1:c.711+1G>A	XP_011515711.1:n.711+1G>A
XM_011517410.1:c.711+1G>A	XP_011515712.1:n.711+1G>A
XM_017014113.2:c.711+1G>A	XP_016869602.1:n.711+1G>A