Canonical Allele Identifier: CA407041095

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411722T>G (hg19) ; chr19:g.50908466T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908466T>G , CM000681.2:g.50908466T>G	GRCh38
NC_000019.9:g.51411722T>G , CM000681.1:g.51411722T>G	GRCh37
NC_000019.8:g.56103534T>G	NCBI36
NG_012154.2:g.7273A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.505A>C MANE Select	ENSP00000326159.1:p.Asn169His
ENST00000324041.5:c.505A>C	ENSP00000326159.1:p.Asn169His
ENST00000431178.2:c.328+113A>C	ENSP00000399448.2:n.328+113A>C
ENST00000593885.1:c.216A>C	ENSP00000469769.1:p.Ter72Cys
ENST00000596876.1:n.507A>C
ENST00000598305.5:c.216A>C	ENSP00000469963.1:p.Ter72Cys
ENST00000599865.5:n.441A>C
ENST00000602148.1:c.517A>C	ENSP00000472091.1:n.517A>C
NM_001302961.1:c.220A>C	NP_001289890.1:p.Asn74His
NM_004917.4:c.505A>C	NP_004908.4:p.Asn169His
NR_126566.1:n.494A>C
XM_005259441.3:c.220A>C	XP_005259498.2:p.Asn74His
XM_011527545.1:c.501A>C	XP_011525847.1:p.Ter167Cys
XM_011527546.1:c.475+113A>C	XP_011525848.1:n.475+113A>C
XM_011527547.1:c.358A>C	XP_011525849.1:p.Asn120His
XM_005259441.4:c.220A>C	XP_005259498.2:p.Asn74His
XM_011527545.3:c.501A>C	XP_011525847.1:p.Ter167Cys
XM_011527546.2:c.475+113A>C	XP_011525848.1:n.475+113A>C
NM_001302961.2:c.220A>C	NP_001289890.1:p.Asn74His
NR_126566.2:n.494A>C
NM_004917.5:c.505A>C MANE Select	NP_004908.4:p.Asn169His