Canonical Allele Identifier: CA15411141

Gene: PRLR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35185478C>T , CM000667.2:g.35185478C>T	GRCh38
NC_000005.9:g.35185580C>T , CM000667.1:g.35185580C>T	GRCh37
NC_000005.8:g.35221337C>T	NCBI36
NG_029042.2:g.50244G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000618457.5:c.-106+44790G>A MANE Select	ENSP00000482954.1:n.-106+44790G>A
ENST00000504500.5:c.-292-32505G>A	ENSP00000422867.1:n.-292-32505G>A
ENST00000508107.5:c.-106+44790G>A	ENSP00000427236.1:n.-106+44790G>A
ENST00000509839.5:c.-106+9625G>A	ENSP00000427060.1:n.-106+9625G>A
ENST00000515839.1:c.-106+10073G>A	ENSP00000421864.1:n.-106+10073G>A
ENST00000618457.4:c.-106+44790G>A	ENSP00000482954.1:n.-106+44790G>A
NM_000949.6:c.-106+44790G>A	NP_000940.1:n.-106+44790G>A
XM_006714484.1:c.-106+9625G>A	XP_006714547.1:n.-106+9625G>A
XM_006714484.2:c.-106+9625G>A	XP_006714547.1:n.-106+9625G>A
XM_017009645.1:c.-186+44790G>A	XP_016865134.1:n.-186+44790G>A
XM_024446131.1:c.59+44790G>A	XP_024301899.1:n.59+44790G>A
XM_024446132.1:c.-106+10073G>A	XP_024301900.1:n.-106+10073G>A
NM_000949.7:c.-106+44790G>A MANE Select	NP_000940.1:n.-106+44790G>A