Canonical Allele Identifier: CA306155016

Gene: MAST3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18110837C>A , CM000681.2:g.18110837C>A	GRCh38
NC_000019.9:g.18221647C>A , CM000681.1:g.18221647C>A	GRCh37
NC_000019.8:g.18082647C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697700.2:c.71+3219C>A	ENSP00000513407.2:n.71+3219C>A
ENST00000697701.1:c.137+96C>A	ENSP00000513408.1:n.137+96C>A
ENST00000704363.1:c.71+3219C>A	ENSP00000515871.1:n.71+3219C>A
ENST00000687212.1:c.161+96C>A MANE Select	ENSP00000509890.1:n.161+96C>A
ENST00000262811.10:c.71+3219C>A	ENSP00000262811.4:n.71+3219C>A
ENST00000608648.1:n.287+96C>A
NM_015016.1:c.71+3219C>A	NP_055831.1:n.71+3219C>A
XM_005259822.2:c.608+96C>A	XP_005259879.2:n.608+96C>A
XM_005259824.2:c.71+3219C>A	XP_005259881.1:n.71+3219C>A
XM_005259825.2:c.71+3219C>A	XP_005259882.1:n.71+3219C>A
XM_006722693.2:c.608+96C>A	XP_006722756.2:n.608+96C>A
XM_006722694.2:c.608+96C>A	XP_006722757.2:n.608+96C>A
XM_006722695.2:c.608+96C>A	XP_006722758.2:n.608+96C>A
XM_006722696.2:c.608+96C>A	XP_006722759.2:n.608+96C>A
XM_006722697.2:c.608+96C>A	XP_006722760.2:n.608+96C>A
XM_006722698.2:c.-178C>A	XP_006722761.1:n.-178C>A
XM_006722699.2:c.353+1186C>A	XP_006722762.2:n.353+1186C>A
XM_011527823.1:c.161+96C>A	XP_011526125.1:n.161+96C>A
XM_017026506.1:c.353+1186C>A	XP_016881995.1:n.353+1186C>A
XM_017026507.1:c.353+1186C>A	XP_016881996.1:n.353+1186C>A
XM_017026508.1:c.353+1186C>A	XP_016881997.1:n.353+1186C>A
XM_017026509.1:c.353+1186C>A	XP_016881998.1:n.353+1186C>A
XM_017026510.2:c.353+1186C>A	XP_016881999.1:n.353+1186C>A
XM_017026511.1:c.137+96C>A	XP_016882000.1:n.137+96C>A
XM_017026512.1:c.71+3219C>A	XP_016882001.1:n.71+3219C>A
XM_017026513.1:c.71+3219C>A	XP_016882002.1:n.71+3219C>A
XM_017026514.1:c.-176+3219C>A	XP_016882003.1:n.-176+3219C>A
XM_017026515.1:c.-175C>A	XP_016882004.1:n.-175C>A
XM_017026516.1:c.353+1186C>A	XP_016882005.1:n.353+1186C>A
NM_015016.2:c.71+3219C>A	NP_055831.1:n.71+3219C>A
NM_001393501.1:c.161+96C>A	NP_001380430.1:n.161+96C>A
NM_001393502.1:c.161+96C>A	NP_001380431.1:n.161+96C>A
NM_001393503.1:c.137+96C>A	NP_001380432.1:n.137+96C>A
NM_001393504.1:c.161+96C>A MANE Select	NP_001380433.1:n.161+96C>A
NM_001393505.1:c.137+96C>A	NP_001380434.1:n.137+96C>A
NM_001393507.1:c.137+96C>A	NP_001380436.1:n.137+96C>A
NM_001393508.1:c.71+3219C>A	NP_001380437.1:n.71+3219C>A
NM_001393509.1:c.71+3219C>A	NP_001380438.1:n.71+3219C>A
NM_001393512.1:c.71+3219C>A	NP_001380441.1:n.71+3219C>A
NM_001393514.1:c.71+3219C>A	NP_001380443.1:n.71+3219C>A
NM_001393515.1:c.71+3219C>A	NP_001380444.1:n.71+3219C>A
NM_001393516.1:c.71+3219C>A	NP_001380445.1:n.71+3219C>A
NM_001393518.1:c.71+3219C>A	NP_001380447.1:n.71+3219C>A
NM_001393520.1:c.71+3219C>A	NP_001380449.1:n.71+3219C>A
NM_001393521.1:c.47+471C>A	NP_001380450.1:n.47+471C>A