Canonical Allele Identifier: CA366981582

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205531T>G (hg19) ; chr7:g.23165912T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165912T>G , CM000669.2:g.23165912T>G	GRCh38
NC_000007.13:g.23205531T>G , CM000669.1:g.23205531T>G	GRCh37
NC_000007.12:g.23172056T>G	NCBI36
NG_016983.1:g.65179T>G
NG_016983.2:g.65179T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1151T>G MANE Select	ENSP00000343273.4:p.Ile384Ser
ENST00000339077.9:c.1151T>G	ENSP00000343273.4:p.Ile384Ser
ENST00000409689.5:c.1007T>G	ENSP00000386263.1:p.Ile336Ser
ENST00000469576.1:n.38T>G
ENST00000521082.5:c.*1159T>G	ENSP00000430351.1:n.*1159T>G
NM_001031710.2:c.1151T>G	NP_001026880.2:p.Ile384Ser
NM_018846.4:c.1007T>G	NP_061334.4:p.Ile336Ser
NR_033328.1:n.1575T>G
XM_006715753.1:c.1190T>G	XP_006715816.1:p.Ile397Ser
XM_006715754.1:c.1124T>G	XP_006715817.1:p.Ile375Ser
XM_006715755.1:c.1124T>G	XP_006715818.1:p.Ile375Ser
XM_006715756.1:c.1046T>G	XP_006715819.1:p.Ile349Ser
XM_006715753.3:c.1190T>G	XP_006715816.1:p.Ile397Ser
XM_006715754.3:c.1124T>G	XP_006715817.1:p.Ile375Ser
XM_006715755.3:c.1124T>G	XP_006715818.1:p.Ile375Ser
XM_006715756.3:c.1046T>G	XP_006715819.1:p.Ile349Ser
XM_017012439.2:c.1085T>G	XP_016867928.1:p.Ile362Ser
NM_001031710.3:c.1151T>G MANE Select	NP_001026880.2:p.Ile384Ser
NM_018846.5:c.1007T>G	NP_061334.4:p.Ile336Ser
NR_033328.2:n.1524T>G