Canonical Allele Identifier: CA2708486547

Gene: PRLR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35064649A>G , CM000667.2:g.35064649A>G	GRCh38
NC_000005.9:g.35064751A>G , CM000667.1:g.35064751A>G	GRCh37
NC_000005.8:g.35100508A>G	NCBI36
NG_029042.2:g.171073T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000949.7:c.*440T>C MANE Select	NP_000940.1:n.*440T>C
ENST00000618457.5:c.*440T>C MANE Select	ENSP00000482954.1:n.*440T>C
NM_000949.6:c.*440T>C	NP_000940.1:n.*440T>C
NM_001204314.2:c.*440T>C	NP_001191243.1:n.*440T>C
NM_001204316.1:c.1009+1300T>C	NP_001191245.1:n.1009+1300T>C
NM_001204317.1:c.855+3567T>C	NP_001191246.1:n.855+3567T>C
NM_001204318.1:c.685+5475T>C	NP_001191247.1:n.685+5475T>C
NR_037910.1:n.827+3567T>C
ENST00000231423.7:c.1009+1300T>C	ENSP00000231423.3:n.1009+1300T>C
ENST00000348262.7:c.685+5475T>C	ENSP00000311613.3:n.685+5475T>C
ENST00000397391.7:c.*447+5475T>C	ENSP00000380546.4:n.*447+5475T>C
ENST00000509140.5:c.855+3567T>C	ENSP00000425300.2:n.855+3567T>C
ENST00000513753.5:c.855+3567T>C	ENSP00000424841.1:n.855+3567T>C
ENST00000514088.5:c.685+5475T>C	ENSP00000422935.2:n.685+5475T>C
ENST00000542609.5:c.1009+1300T>C	ENSP00000441813.2:n.1009+1300T>C
ENST00000618457.4:c.*440T>C	ENSP00000482954.1:n.*440T>C
ENST00000618625.4:c.*617+3567T>C	ENSP00000479077.1:n.*617+3567T>C
ENST00000620785.4:c.*440T>C	ENSP00000482689.1:n.*440T>C
XM_006714484.1:c.*440T>C	XP_006714547.1:n.*440T>C
XM_006714484.2:c.*440T>C	XP_006714547.1:n.*440T>C
XM_011514068.1:c.*440T>C	XP_011512370.1:n.*440T>C
XM_011514068.2:c.*440T>C	XP_011512370.1:n.*440T>C
XM_011514069.1:c.*440T>C	XP_011512371.1:n.*440T>C
XM_011514069.2:c.*440T>C	XP_011512371.1:n.*440T>C
XM_017009645.1:c.*440T>C	XP_016865134.1:n.*440T>C
XM_024446131.1:c.*440T>C	XP_024301899.1:n.*440T>C
XM_024446132.1:c.*440T>C	XP_024301900.1:n.*440T>C