Canonical Allele Identifier: CA810121914

Gene: PRLR

Linked Data

• dbSNP Id: rs10075993
• MyVariant Identifiers: chr5:g.35186373A>C (hg19) ; chr5:g.35186271A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35186271A>C , CM000667.2:g.35186271A>C	GRCh38
NC_000005.9:g.35186373A>C , CM000667.1:g.35186373A>C	GRCh37
NC_000005.8:g.35222130A>C	NCBI36
NG_029042.2:g.49451T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000618457.5:c.-106+43997T>G MANE Select	ENSP00000482954.1:n.-106+43997T>G
ENST00000504500.5:c.-292-33298T>G	ENSP00000422867.1:n.-292-33298T>G
ENST00000508107.5:c.-106+43997T>G	ENSP00000427236.1:n.-106+43997T>G
ENST00000509839.5:c.-106+8832T>G	ENSP00000427060.1:n.-106+8832T>G
ENST00000515839.1:c.-106+9280T>G	ENSP00000421864.1:n.-106+9280T>G
ENST00000618457.4:c.-106+43997T>G	ENSP00000482954.1:n.-106+43997T>G
NM_000949.6:c.-106+43997T>G	NP_000940.1:n.-106+43997T>G
XM_006714484.1:c.-106+8832T>G	XP_006714547.1:n.-106+8832T>G
XM_006714484.2:c.-106+8832T>G	XP_006714547.1:n.-106+8832T>G
XM_017009645.1:c.-186+43997T>G	XP_016865134.1:n.-186+43997T>G
XM_024446131.1:c.59+43997T>G	XP_024301899.1:n.59+43997T>G
XM_024446132.1:c.-106+9280T>G	XP_024301900.1:n.-106+9280T>G
NM_000949.7:c.-106+43997T>G MANE Select	NP_000940.1:n.-106+43997T>G