Canonical Allele Identifier: CA408207073

Gene: PLCB1

Linked Data

• COSMIC: COSM1713177 ; COSM1713178 ; COSM3549431
• MyVariant Identifiers: chr20:g.8717804C>T (hg19) ; chr20:g.8737157C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.8737157C>T , CM000682.2:g.8737157C>T	GRCh38
NC_000020.10:g.8717804C>T , CM000682.1:g.8717804C>T	GRCh37
NC_000020.9:g.8665804C>T	NCBI36
NG_028168.1:g.609509C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338037.11:c.2173C>T MANE Select	ENSP00000338185.6:p.Pro725Ser
ENST00000635830.1:n.2244C>T
ENST00000636825.1:n.2037C>T
ENST00000637919.1:c.1870C>T	ENSP00000490862.1:p.Pro624Ser
ENST00000338037.10:c.2173C>T	ENSP00000338185.6:p.Pro725Ser
ENST00000378637.6:c.2173C>T	ENSP00000367904.2:p.Pro725Ser
ENST00000378641.7:c.2173C>T	ENSP00000367908.3:p.Pro725Ser
ENST00000439627.2:c.130C>T	ENSP00000391162.1:p.Pro44Ser
ENST00000487210.5:c.1395C>T
ENST00000494924.2:n.1325C>T
ENST00000612075.4:c.1933C>T	ENSP00000479997.1:p.Pro645Ser
ENST00000617005.4:c.1933C>T	ENSP00000477664.1:p.Pro645Ser
ENST00000625874.2:c.1870C>T	ENSP00000486301.1:p.Pro624Ser
ENST00000626966.2:c.1870C>T	ENSP00000487075.1:p.Pro624Ser
NM_015192.3:c.2173C>T	NP_056007.1:p.Pro725Ser
NM_182734.2:c.2173C>T	NP_877398.1:p.Pro725Ser
XM_011529199.1:c.2173C>T	XP_011527501.1:p.Pro725Ser
XM_011529200.1:c.1957C>T	XP_011527502.1:p.Pro653Ser
XM_011529201.1:c.1870C>T	XP_011527503.1:p.Pro624Ser
XM_011529203.1:c.400C>T	XP_011527505.1:p.Pro134Ser
NM_015192.4:c.2173C>T MANE Select	NP_056007.1:p.Pro725Ser
NM_182734.3:c.2173C>T	NP_877398.1:p.Pro725Ser