Canonical Allele Identifier: CA876298074

Gene: HUWE1

Linked Data

• dbSNP Id: rs1159163890
• gnomAD v4: X-53625130-CAA-C
• MyVariant Identifiers: chrX:g.53625131_53625132del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53625136_53625137del , CM000685.2:g.53625136_53625137del	GRCh38
NC_000023.10:g.53652097_53652098del , CM000685.1:g.53652097_53652098del	GRCh37
NC_000023.9:g.53668822_53668823del	NCBI36
NG_016261.2:g.66602_66603del

Transcript Alleles

HGVS	Amino-acid change
ENST00000704099.1:c.1591+25_1591+26del	ENSP00000515693.1:n.1591+25_1591+26del
ENST00000704100.1:c.1591+25_1591+26del	ENSP00000515694.1:n.1591+25_1591+26del
ENST00000262854.11:c.1591+25_1591+26del MANE Select	ENSP00000262854.6:n.1591+25_1591+26del
ENST00000218328.12:n.1993+25_1993+26del
ENST00000262854.10:c.1591+25_1591+26del	ENSP00000262854.6:n.1591+25_1591+26del
ENST00000342160.7:c.1591+25_1591+26del	ENSP00000340648.3:n.1591+25_1591+26del
ENST00000489876.1:n.322+25_322+26del
ENST00000612484.4:c.1591+25_1591+26del	ENSP00000479451.1:n.1591+25_1591+26del
ENST00000622887.1:c.632+25_632+26del
NM_031407.6:c.1591+25_1591+26del	NP_113584.3:n.1591+25_1591+26del
XM_005261965.2:c.1591+25_1591+26del	XP_005262022.1:n.1591+25_1591+26del
XM_011530746.1:c.1840+25_1840+26del	XP_011529048.1:n.1840+25_1840+26del
XM_011530747.1:c.1840+25_1840+26del	XP_011529049.1:n.1840+25_1840+26del
XM_011530748.1:c.1840+25_1840+26del	XP_011529050.1:n.1840+25_1840+26del
XM_011530749.1:c.1840+25_1840+26del	XP_011529051.1:n.1840+25_1840+26del
XM_011530750.1:c.1840+25_1840+26del	XP_011529052.1:n.1840+25_1840+26del
XM_011530751.1:c.1840+25_1840+26del	XP_011529053.1:n.1840+25_1840+26del
XM_011530752.1:c.1840+25_1840+26del	XP_011529054.1:n.1840+25_1840+26del
XM_011530753.1:c.1840+25_1840+26del	XP_011529055.1:n.1840+25_1840+26del
XM_011530754.1:c.1840+25_1840+26del	XP_011529056.1:n.1840+25_1840+26del
XM_011530755.1:c.1840+25_1840+26del	XP_011529057.1:n.1840+25_1840+26del
XM_011530756.1:c.1840+25_1840+26del	XP_011529058.1:n.1840+25_1840+26del
XM_011530757.1:c.1840+25_1840+26del	XP_011529059.1:n.1840+25_1840+26del
XM_011530758.1:c.1840+25_1840+26del	XP_011529060.1:n.1840+25_1840+26del
XR_938360.1:n.2275+25_2275+26del
XM_005261965.4:c.1591+25_1591+26del	XP_005262022.1:n.1591+25_1591+26del
XM_011530751.2:c.1840+25_1840+26del	XP_011529053.1:n.1840+25_1840+26del
XM_017029191.1:c.1972+25_1972+26del	XP_016884680.1:n.1972+25_1972+26del
XM_017029192.1:c.1972+25_1972+26del	XP_016884681.1:n.1972+25_1972+26del
XM_017029193.1:c.1951+25_1951+26del	XP_016884682.1:n.1951+25_1951+26del
XM_017029194.1:c.1972+25_1972+26del	XP_016884683.1:n.1972+25_1972+26del
XM_017029195.1:c.1972+25_1972+26del	XP_016884684.1:n.1972+25_1972+26del
XM_017029196.1:c.1972+25_1972+26del	XP_016884685.1:n.1972+25_1972+26del
XM_017029197.1:c.1972+25_1972+26del	XP_016884686.1:n.1972+25_1972+26del
XM_017029198.2:c.1861+25_1861+26del	XP_016884687.1:n.1861+25_1861+26del
XM_017029199.1:c.1861+25_1861+26del	XP_016884688.1:n.1861+25_1861+26del
XM_017029200.1:c.1861+25_1861+26del	XP_016884689.1:n.1861+25_1861+26del
XM_017029201.1:c.1861+25_1861+26del	XP_016884690.1:n.1861+25_1861+26del
XM_017029202.1:c.1861+25_1861+26del	XP_016884691.1:n.1861+25_1861+26del
XM_017029203.1:c.1861+25_1861+26del	XP_016884692.1:n.1861+25_1861+26del
XM_017029204.1:c.1723+25_1723+26del	XP_016884693.1:n.1723+25_1723+26del
XM_017029206.1:c.1972+25_1972+26del	XP_016884695.1:n.1972+25_1972+26del
XM_024452322.1:c.1840+25_1840+26del	XP_024308090.1:n.1840+25_1840+26del
NM_031407.7:c.1591+25_1591+26del MANE Select	NP_113584.3:n.1591+25_1591+26del