Canonical Allele Identifier: CA263645784

Gene: YLPM1

Linked Data

• dbSNP Id: rs954412463
• gnomAD v3: 14-74809794-C-T
• gnomAD v4: 14-74809794-C-T
• COSMIC: COSM5748496 ; COSM5748497
• MyVariant Identifiers: chr14:g.75276497C>T (hg19) ; chr14:g.74809794C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74809794C>T , CM000676.2:g.74809794C>T	GRCh38
NC_000014.8:g.75276497C>T , CM000676.1:g.75276497C>T	GRCh37
NC_000014.7:g.74346250C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325680.12:c.4936C>T MANE Select	ENSP00000324463.7:p.Arg1646Ter
ENST00000325680.11:c.4936C>T	ENSP00000324463.7:p.Arg1646Ter
ENST00000547879.5:c.163C>T	ENSP00000448367.1:p.Arg55Ter
ENST00000549293.5:c.3595C>T	ENSP00000449860.1:p.Arg1199Ter
ENST00000552421.5:c.2818C>T	ENSP00000447921.1:p.Arg940Ter
NM_019589.2:c.4936C>T	NP_062535.2:p.Arg1646Ter
XM_005267860.3:c.4936C>T	XP_005267917.1:p.Arg1646Ter
XM_011536966.1:c.3721C>T	XP_011535268.1:p.Arg1241Ter
XM_011536967.1:c.2818C>T	XP_011535269.1:p.Arg940Ter
XR_943494.1:n.5104C>T
XM_005267860.4:c.4936C>T	XP_005267917.1:p.Arg1646Ter
XM_011536966.2:c.3721C>T	XP_011535268.1:p.Arg1241Ter
XM_011536967.2:c.2818C>T	XP_011535269.1:p.Arg940Ter
XR_001750436.2:n.5110C>T
NM_019589.3:c.4936C>T MANE Select	NP_062535.2:p.Arg1646Ter