Canonical Allele Identifier: CA366981382

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205443T>G (hg19) ; chr7:g.23165824T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165824T>G , CM000669.2:g.23165824T>G	GRCh38
NC_000007.13:g.23205443T>G , CM000669.1:g.23205443T>G	GRCh37
NC_000007.12:g.23171968T>G	NCBI36
NG_016983.1:g.65091T>G
NG_016983.2:g.65091T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1063T>G MANE Select	ENSP00000343273.4:p.Tyr355Asp
ENST00000339077.9:c.1063T>G	ENSP00000343273.4:p.Tyr355Asp
ENST00000409689.5:c.919T>G	ENSP00000386263.1:p.Tyr307Asp
ENST00000521082.5:c.*1071T>G	ENSP00000430351.1:n.*1071T>G
NM_001031710.2:c.1063T>G	NP_001026880.2:p.Tyr355Asp
NM_018846.4:c.919T>G	NP_061334.4:p.Tyr307Asp
NR_033328.1:n.1487T>G
XM_006715753.1:c.1102T>G	XP_006715816.1:p.Tyr368Asp
XM_006715754.1:c.1036T>G	XP_006715817.1:p.Tyr346Asp
XM_006715755.1:c.1036T>G	XP_006715818.1:p.Tyr346Asp
XM_006715756.1:c.958T>G	XP_006715819.1:p.Tyr320Asp
XM_006715753.3:c.1102T>G	XP_006715816.1:p.Tyr368Asp
XM_006715754.3:c.1036T>G	XP_006715817.1:p.Tyr346Asp
XM_006715755.3:c.1036T>G	XP_006715818.1:p.Tyr346Asp
XM_006715756.3:c.958T>G	XP_006715819.1:p.Tyr320Asp
XM_017012439.2:c.997T>G	XP_016867928.1:p.Tyr333Asp
NM_001031710.3:c.1063T>G MANE Select	NP_001026880.2:p.Tyr355Asp
NM_018846.5:c.919T>G	NP_061334.4:p.Tyr307Asp
NR_033328.2:n.1436T>G