Canonical Allele Identifier: CA371302753

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61769418A>T (hg19) ; chr8:g.60856859A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60856859A>T , CM000670.2:g.60856859A>T	GRCh38
NC_000008.10:g.61769418A>T , CM000670.1:g.61769418A>T	GRCh37
NC_000008.9:g.61931972A>T	NCBI36
NG_007009.1:g.183080A>T , LRG_176:g.183080A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.755A>T
ENST00000695853.1:c.*638A>T	ENSP00000512218.1:n.*638A>T
ENST00000423902.7:c.7579A>T MANE Select	ENSP00000392028.1:p.Met2527Leu
ENST00000423902.6:c.7579A>T	ENSP00000392028.1:p.Met2527Leu
ENST00000524602.5:c.1717-5370A>T	ENSP00000437061.1:n.1717-5370A>T
ENST00000529472.1:n.760A>T
ENST00000531695.1:n.3A>T
NM_001316690.1:c.1717-5370A>T	NP_001303619.1:n.1717-5370A>T
NM_017780.3:c.7579A>T	NP_060250.2:p.Met2527Leu
XM_011517553.1:c.7669A>T	XP_011515855.1:p.Met2557Leu
XM_011517554.1:c.7669A>T	XP_011515856.1:p.Met2557Leu
XM_011517555.1:c.7666A>T	XP_011515857.1:p.Met2556Leu
XM_011517556.1:c.7669A>T	XP_011515858.1:p.Met2557Leu
XM_011517557.1:c.5656A>T	XP_011515859.1:p.Met1886Leu
XM_011517558.1:c.5206A>T	XP_011515860.1:p.Met1736Leu
XM_011517559.1:c.4414A>T	XP_011515861.1:p.Met1472Leu
XM_011517553.2:c.7669A>T	XP_011515855.1:p.Met2557Leu
XM_011517554.3:c.7669A>T	XP_011515856.1:p.Met2557Leu
XM_011517555.2:c.7666A>T	XP_011515857.1:p.Met2556Leu
XM_017013612.1:c.7669A>T	XP_016869101.1:p.Met2557Leu
XM_017013613.1:c.7576A>T	XP_016869102.1:p.Met2526Leu
NM_017780.4:c.7579A>T MANE Select	NP_060250.2:p.Met2527Leu