Canonical Allele Identifier: CA2830540451

Gene: PRL

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.22292822_22292834del , CM000668.2:g.22292822_22292834del	GRCh38
NC_000006.11:g.22293051_22293063del , CM000668.1:g.22293051_22293063del	GRCh37
NC_000006.10:g.22401030_22401042del	NCBI36
NG_029819.1:g.15020_15032del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306482.2:c.205-189_205-177del MANE Select	ENSP00000302150.1:n.205-189_205-177del
ENST00000651245.1:c.205-189_205-177del	ENSP00000498773.1:n.205-189_205-177del
ENST00000651757.1:c.205-189_205-177del	ENSP00000499154.1:n.205-189_205-177del
ENST00000306482.1:c.205-189_205-177del	ENSP00000302150.1:n.205-189_205-177del
ENST00000615510.4:c.112-189_112-177del	ENSP00000478566.1:n.112-189_112-177del
ENST00000617911.4:c.208-189_208-177del	ENSP00000480195.1:n.208-189_208-177del
NM_000948.5:c.205-189_205-177del	NP_000939.1:n.205-189_205-177del
NM_001163558.2:c.205-189_205-177del	NP_001157030.1:n.205-189_205-177del
XM_011514753.1:c.208-189_208-177del	XP_011513055.1:n.208-189_208-177del
XM_011514754.1:c.208-189_208-177del	XP_011513056.1:n.208-189_208-177del
XM_011514753.2:c.208-189_208-177del	XP_011513055.1:n.208-189_208-177del
XM_011514754.2:c.208-189_208-177del	XP_011513056.1:n.208-189_208-177del
NM_000948.6:c.205-189_205-177del MANE Select	NP_000939.1:n.205-189_205-177del
NM_001163558.3:c.205-189_205-177del	NP_001157030.1:n.205-189_205-177del