Canonical Allele Identifier: CA359986616

Gene: MCCC2

Linked Data

• MyVariant Identifiers: chr5:g.70930813G>T (hg19) ; chr5:g.71634986G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71634986G>T , CM000667.2:g.71634986G>T	GRCh38
NC_000005.9:g.70930813G>T , CM000667.1:g.70930813G>T	GRCh37
NC_000005.8:g.70966569G>T	NCBI36
NG_008882.1:g.52699G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000505435.4:n.803G>T
ENST00000505787.8:n.2687G>T
ENST00000509358.7:c.847G>T	ENSP00000420994.3:p.Ala283Ser
ENST00000509539.3:c.109G>T	ENSP00000425474.3:p.Ala37Ser
ENST00000510895.7:n.970G>T
ENST00000629193.3:c.733G>T	ENSP00000486535.2:p.Ala245Ser
ENST00000681968.1:c.340G>T	ENSP00000508143.1:p.Ala114Ser
ENST00000682045.1:c.703G>T	ENSP00000507329.1:p.Ala235Ser
ENST00000682214.1:c.454G>T	ENSP00000507336.1:p.Ala152Ser
ENST00000682499.1:n.1668G>T
ENST00000682541.1:c.847G>T	ENSP00000507673.1:p.Ala283Ser
ENST00000682687.1:c.847G>T	ENSP00000507945.1:p.Ala283Ser
ENST00000682727.1:c.847G>T	ENSP00000507393.1:p.Ala283Ser
ENST00000682876.1:c.976G>T	ENSP00000508389.1:p.Ala326Ser
ENST00000683098.1:c.803+2801G>T	ENSP00000507670.1:n.803+2801G>T
ENST00000683258.1:c.*568G>T	ENSP00000507448.1:n.*568G>T
ENST00000683339.1:c.631G>T	ENSP00000507758.1:p.Ala211Ser
ENST00000683403.1:c.813+34G>T	ENSP00000507896.1:n.813+34G>T
ENST00000683429.1:c.454G>T	ENSP00000507697.1:p.Ala152Ser
ENST00000683665.1:c.847G>T	ENSP00000507068.1:p.Ala283Ser
ENST00000683789.1:c.733G>T	ENSP00000507012.1:p.Ala245Ser
ENST00000683847.1:n.691G>T
ENST00000683882.1:c.847G>T	ENSP00000506735.1:p.Ala283Ser
ENST00000684024.1:c.*518G>T	ENSP00000507175.1:n.*518G>T
ENST00000684254.1:c.*573G>T	ENSP00000508001.1:n.*573G>T
ENST00000684310.1:c.109G>T	ENSP00000507550.1:p.Ala37Ser
ENST00000684530.1:c.109G>T	ENSP00000507439.1:p.Ala37Ser
ENST00000684652.1:n.1849G>T
ENST00000340941.11:c.847G>T MANE Select	ENSP00000343657.6:p.Ala283Ser
ENST00000340941.10:c.847G>T	ENSP00000343657.6:p.Ala283Ser
ENST00000505435.3:n.198G>T
ENST00000505787.7:n.661G>T
ENST00000509358.6:c.847G>T	ENSP00000420994.2:p.Ala283Ser
ENST00000509539.2:c.172G>T	ENSP00000425474.2:p.Ala58Ser
ENST00000510895.6:n.461G>T
ENST00000512218.6:c.733G>T	ENSP00000423202.2:p.Ala245Ser
ENST00000629193.2:c.733G>T	ENSP00000486535.1:p.Ala245Ser
NM_022132.4:c.847G>T	NP_071415.1:p.Ala283Ser
XM_005248567.1:c.733G>T	XP_005248624.1:p.Ala245Ser
XM_011543528.1:c.847G>T	XP_011541830.1:p.Ala283Ser
XM_011543529.1:c.847G>T	XP_011541831.1:p.Ala283Ser
NM_001363147.1:c.733G>T	NP_001350076.1:p.Ala245Ser
XM_011543529.2:c.847G>T	XP_011541831.1:p.Ala283Ser
XM_017009688.1:c.847G>T	XP_016865177.1:p.Ala283Ser
XR_001742172.1:n.887G>T
NM_022132.5:c.847G>T MANE Select	NP_071415.1:p.Ala283Ser