Canonical Allele Identifier: CA372190112
Community Standard Title: NM_014846.4(WASHC5):c.2087G>A (p.Gly696Asp)
Gene: WASHC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125055601C>T , CM000670.2:g.125055601C>T GRCh38
NC_000008.10:g.126067843C>T , CM000670.1:g.126067843C>T GRCh37
NC_000008.9:g.126137025C>T NCBI36
NG_012636.1:g.41219G>A

Transcript Alleles

HGVS Amino-acid Change
NM_014846.4:c.2087G>A MANE Select NP_055661.3:p.Gly696Asp
ENST00000318410.12:c.2087G>A MANE Select ENSP00000318016.7:p.Gly696Asp
NM_001330609.1:c.1643G>A NP_001317538.1:p.Gly548Asp
NM_001330609.2:c.1643G>A NP_001317538.1:p.Gly548Asp
NM_014846.3:c.2087G>A NP_055661.3:p.Gly696Asp
ENST00000318410.11:c.2087G>A ENSP00000318016.7:p.Gly696Asp
ENST00000517845.5:c.1643G>A ENSP00000429676.1:p.Gly548Asp
XM_005251120.2:c.1643G>A XP_005251177.1:p.Gly548Asp
XM_011517409.1:c.2087G>A XP_011515711.1:p.Gly696Asp
XM_011517410.1:c.2087G>A XP_011515712.1:p.Gly696Asp
XM_017014113.2:c.2087G>A XP_016869602.1:p.Gly696Asp