Canonical Allele Identifier: CA415087740

Gene: CCNQ

Linked Data

• MyVariant Identifiers: chrX:g.152858053G>C (hg19) ; chrX:g.153592595G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592595G>C , CM000685.2:g.153592595G>C	GRCh38
NC_000023.10:g.152858053G>C , CM000685.1:g.152858053G>C	GRCh37
NC_000023.9:g.152511247G>C	NCBI36
NG_008393.2:g.11583C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.568C>G MANE Select	ENSP00000461135.1:p.His190Asp
ENST00000429336.5:c.193+1952C>G
ENST00000440428.5:c.568C>G	ENSP00000402949.2:p.His190Asp
ENST00000576892.7:c.568C>G	ENSP00000461135.1:p.His190Asp
ENST00000614850.1:c.277+3409C>G
ENST00000614851.4:c.389C>G
ENST00000620088.4:c.*444C>G	ENSP00000484108.1:n.*444C>G
ENST00000621629.4:c.*444C>G	ENSP00000478747.1:n.*444C>G
ENST00000621817.1:c.*733C>G	ENSP00000481634.1:n.*733C>G
NM_001130997.2:c.568C>G	NP_001124469.1:p.His190Asp
NM_152274.4:c.568C>G	NP_689487.2:p.His190Asp
XM_005277920.3:c.538C>G	XP_005277977.1:p.His180Asp
XM_005277921.3:c.538C>G	XP_005277978.1:p.His180Asp
XM_011531213.1:c.442C>G	XP_011529515.1:p.His148Asp
XM_011531214.1:c.442C>G	XP_011529516.1:p.His148Asp
XM_011531215.1:c.442C>G	XP_011529517.1:p.His148Asp
XM_005277920.4:c.538C>G	XP_005277977.1:p.His180Asp
XM_005277921.4:c.538C>G	XP_005277978.1:p.His180Asp
XM_011531214.2:c.442C>G	XP_011529516.1:p.His148Asp
XM_011531215.2:c.442C>G	XP_011529517.1:p.His148Asp
XR_002958810.1:n.2473C>G
NM_152274.5:c.568C>G MANE Select	NP_689487.2:p.His190Asp
NM_001130997.3:c.568C>G	NP_001124469.1:p.His190Asp