Canonical Allele Identifier: CA407041723

Gene: KLK4

Linked Data

• gnomAD v4: 19-50908755-C-G
• MyVariant Identifiers: chr19:g.51412011C>G (hg19) ; chr19:g.50908755C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908755C>G , CM000681.2:g.50908755C>G	GRCh38
NC_000019.9:g.51412011C>G , CM000681.1:g.51412011C>G	GRCh37
NC_000019.8:g.56103823C>G	NCBI36
NG_012154.2:g.6984G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.299G>C MANE Select	ENSP00000326159.1:p.Ser100Thr
ENST00000324041.5:c.299G>C	ENSP00000326159.1:p.Ser100Thr
ENST00000431178.2:c.152G>C	ENSP00000399448.2:p.Ser51Thr
ENST00000593885.1:c.14G>C	ENSP00000469769.1:p.Ser5Thr
ENST00000596876.1:n.218G>C
ENST00000598305.5:c.14G>C	ENSP00000469963.1:p.Ser5Thr
ENST00000599865.5:n.152G>C
ENST00000602148.1:c.311G>C	ENSP00000472091.1:n.311G>C
NM_001302961.1:c.14G>C	NP_001289890.1:p.Ser5Thr
NM_004917.4:c.299G>C	NP_004908.4:p.Ser100Thr
NR_126566.1:n.292G>C
XM_005259441.3:c.14G>C	XP_005259498.2:p.Ser5Thr
XM_011527545.1:c.299G>C	XP_011525847.1:p.Ser100Thr
XM_011527546.1:c.299G>C	XP_011525848.1:p.Ser100Thr
XM_011527547.1:c.152G>C	XP_011525849.1:p.Ser51Thr
XM_005259441.4:c.14G>C	XP_005259498.2:p.Ser5Thr
XM_011527545.3:c.299G>C	XP_011525847.1:p.Ser100Thr
XM_011527546.2:c.299G>C	XP_011525848.1:p.Ser100Thr
NM_001302961.2:c.14G>C	NP_001289890.1:p.Ser5Thr
NR_126566.2:n.292G>C
NM_004917.5:c.299G>C MANE Select	NP_004908.4:p.Ser100Thr