Canonical Allele Identifier: CA15411142

Gene: PRLR

Linked Data

• dbSNP Id: rs10075993
• gnomAD v2: 5-35186373-A-T
• gnomAD v3: 5-35186271-A-T
• gnomAD v4: 5-35186271-A-T
• MyVariant Identifiers: chr5:g.35186373A>T (hg19) ; chr5:g.35186271A>T (hg38)

Genomic Alleles

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

Transcript Alleles

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