Canonical Allele Identifier: CA1538760256

Gene: PRLR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35186306T= , CM000667.2:g.35186306T=	GRCh38
NC_000005.9:g.35186408T= , CM000667.1:g.35186408T=	GRCh37
NC_000005.8:g.35222165T=	NCBI36
NG_029042.2:g.49416A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000618457.5:c.-106+43962A= MANE Select	ENSP00000482954.1:n.-106+43962A=
ENST00000504500.5:c.-292-33333A=	ENSP00000422867.1:n.-292-33333A=
ENST00000508107.5:c.-106+43962A=	ENSP00000427236.1:n.-106+43962A=
ENST00000509839.5:c.-106+8797A=	ENSP00000427060.1:n.-106+8797A=
ENST00000515839.1:c.-106+9245A=	ENSP00000421864.1:n.-106+9245A=
ENST00000618457.4:c.-106+43962A=	ENSP00000482954.1:n.-106+43962A=
NM_000949.6:c.-106+43962A=	NP_000940.1:n.-106+43962A=
XM_006714484.1:c.-106+8797A=	XP_006714547.1:n.-106+8797A=
XM_006714484.2:c.-106+8797A=	XP_006714547.1:n.-106+8797A=
XM_017009645.1:c.-186+43962A=	XP_016865134.1:n.-186+43962A=
XM_024446131.1:c.59+43962A=	XP_024301899.1:n.59+43962A=
XM_024446132.1:c.-106+9245A=	XP_024301900.1:n.-106+9245A=
NM_000949.7:c.-106+43962A= MANE Select	NP_000940.1:n.-106+43962A=