Canonical Allele Identifier: CA359987228

Gene: MCCC2

Linked Data

• MyVariant Identifiers: chr5:g.70930868A>C (hg19) ; chr5:g.71635041A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635041A>C , CM000667.2:g.71635041A>C	GRCh38
NC_000005.9:g.70930868A>C , CM000667.1:g.70930868A>C	GRCh37
NC_000005.8:g.70966624A>C	NCBI36
NG_008882.1:g.52754A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.858A>C
ENST00000505787.8:n.2742A>C
ENST00000509358.7:c.902A>C	ENSP00000420994.3:p.Asp301Ala
ENST00000509539.3:c.164A>C	ENSP00000425474.3:p.Asp55Ala
ENST00000510895.7:n.1025A>C
ENST00000629193.3:c.788A>C	ENSP00000486535.2:p.Asp263Ala
ENST00000681968.1:c.395A>C	ENSP00000508143.1:p.Asp132Ala
ENST00000682045.1:c.758A>C	ENSP00000507329.1:p.Asp253Ala
ENST00000682214.1:c.509A>C	ENSP00000507336.1:p.Asp170Ala
ENST00000682499.1:n.1723A>C
ENST00000682541.1:c.902A>C	ENSP00000507673.1:p.Asp301Ala
ENST00000682687.1:c.902A>C	ENSP00000507945.1:p.Asp301Ala
ENST00000682727.1:c.902A>C	ENSP00000507393.1:p.Asp301Ala
ENST00000682876.1:c.1031A>C	ENSP00000508389.1:p.Asp344Ala
ENST00000683098.1:c.803+2856A>C	ENSP00000507670.1:n.803+2856A>C
ENST00000683258.1:c.*623A>C	ENSP00000507448.1:n.*623A>C
ENST00000683339.1:c.686A>C	ENSP00000507758.1:p.Asp229Ala
ENST00000683403.1:c.813+89A>C	ENSP00000507896.1:n.813+89A>C
ENST00000683429.1:c.509A>C	ENSP00000507697.1:p.Asp170Ala
ENST00000683665.1:c.902A>C	ENSP00000507068.1:p.Asp301Ala
ENST00000683789.1:c.788A>C	ENSP00000507012.1:p.Asp263Ala
ENST00000683847.1:n.746A>C
ENST00000683882.1:c.902A>C	ENSP00000506735.1:p.Asp301Ala
ENST00000684024.1:c.*573A>C	ENSP00000507175.1:n.*573A>C
ENST00000684254.1:c.*628A>C	ENSP00000508001.1:n.*628A>C
ENST00000684310.1:c.164A>C	ENSP00000507550.1:p.Asp55Ala
ENST00000684530.1:c.164A>C	ENSP00000507439.1:p.Asp55Ala
ENST00000684652.1:n.1904A>C
ENST00000340941.11:c.902A>C MANE Select	ENSP00000343657.6:p.Asp301Ala
ENST00000340941.10:c.902A>C	ENSP00000343657.6:p.Asp301Ala
ENST00000505435.3:n.253A>C
ENST00000505787.7:n.716A>C
ENST00000509358.6:c.902A>C	ENSP00000420994.2:p.Asp301Ala
ENST00000509539.2:c.227A>C	ENSP00000425474.2:p.Asp76Ala
ENST00000510895.6:n.516A>C
ENST00000512218.6:c.788A>C	ENSP00000423202.2:p.Asp263Ala
ENST00000629193.2:c.788A>C	ENSP00000486535.1:p.Asp263Ala
NM_022132.4:c.902A>C	NP_071415.1:p.Asp301Ala
XM_005248567.1:c.788A>C	XP_005248624.1:p.Asp263Ala
XM_011543528.1:c.902A>C	XP_011541830.1:p.Asp301Ala
XM_011543529.1:c.902A>C	XP_011541831.1:p.Asp301Ala
NM_001363147.1:c.788A>C	NP_001350076.1:p.Asp263Ala
XM_011543529.2:c.902A>C	XP_011541831.1:p.Asp301Ala
XM_017009688.1:c.902A>C	XP_016865177.1:p.Asp301Ala
XR_001742172.1:n.942A>C
NM_022132.5:c.902A>C MANE Select	NP_071415.1:p.Asp301Ala