Canonical Allele Identifier: CA1538760247

Gene: PRLR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35186286A= , CM000667.2:g.35186286A=	GRCh38
NC_000005.9:g.35186388A= , CM000667.1:g.35186388A=	GRCh37
NC_000005.8:g.35222145A=	NCBI36
NG_029042.2:g.49436T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000618457.5:c.-106+43982T= MANE Select	ENSP00000482954.1:n.-106+43982T=
ENST00000504500.5:c.-292-33313T=	ENSP00000422867.1:n.-292-33313T=
ENST00000508107.5:c.-106+43982T=	ENSP00000427236.1:n.-106+43982T=
ENST00000509839.5:c.-106+8817T=	ENSP00000427060.1:n.-106+8817T=
ENST00000515839.1:c.-106+9265T=	ENSP00000421864.1:n.-106+9265T=
ENST00000618457.4:c.-106+43982T=	ENSP00000482954.1:n.-106+43982T=
NM_000949.6:c.-106+43982T=	NP_000940.1:n.-106+43982T=
XM_006714484.1:c.-106+8817T=	XP_006714547.1:n.-106+8817T=
XM_006714484.2:c.-106+8817T=	XP_006714547.1:n.-106+8817T=
XM_017009645.1:c.-186+43982T=	XP_016865134.1:n.-186+43982T=
XM_024446131.1:c.59+43982T=	XP_024301899.1:n.59+43982T=
XM_024446132.1:c.-106+9265T=	XP_024301900.1:n.-106+9265T=
NM_000949.7:c.-106+43982T= MANE Select	NP_000940.1:n.-106+43982T=