Canonical Allele Identifier: CA1554387665

Gene: MCCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71634872A= , CM000667.2:g.71634872A=	GRCh38
NC_000005.9:g.70930699A= , CM000667.1:g.70930699A=	GRCh37
NC_000005.8:g.70966455A=	NCBI36
NG_008882.1:g.52585A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.760-71A=
ENST00000505787.8:n.2644-71A=
ENST00000509358.7:c.804-71A=	ENSP00000420994.3:n.804-71A=
ENST00000509539.3:c.66-71A=	ENSP00000425474.3:n.66-71A=
ENST00000510895.7:n.927-71A=
ENST00000629193.3:c.690-71A=	ENSP00000486535.2:n.690-71A=
ENST00000681968.1:c.297-71A=	ENSP00000508143.1:n.297-71A=
ENST00000682045.1:c.660-71A=	ENSP00000507329.1:n.660-71A=
ENST00000682214.1:c.411-71A=	ENSP00000507336.1:n.411-71A=
ENST00000682499.1:n.1625-71A=
ENST00000682541.1:c.804-71A=	ENSP00000507673.1:n.804-71A=
ENST00000682687.1:c.804-71A=	ENSP00000507945.1:n.804-71A=
ENST00000682727.1:c.804-71A=	ENSP00000507393.1:n.804-71A=
ENST00000682876.1:c.933-71A=	ENSP00000508389.1:n.933-71A=
ENST00000683098.1:c.803+2687A=	ENSP00000507670.1:n.803+2687A=
ENST00000683258.1:c.*525-71A=	ENSP00000507448.1:n.*525-71A=
ENST00000683339.1:c.588-71A=	ENSP00000507758.1:n.588-71A=
ENST00000683403.1:c.804-71A=	ENSP00000507896.1:n.804-71A=
ENST00000683429.1:c.411-71A=	ENSP00000507697.1:n.411-71A=
ENST00000683665.1:c.804-71A=	ENSP00000507068.1:n.804-71A=
ENST00000683789.1:c.690-71A=	ENSP00000507012.1:n.690-71A=
ENST00000683847.1:n.648-71A=
ENST00000683882.1:c.804-71A=	ENSP00000506735.1:n.804-71A=
ENST00000684024.1:c.*475-71A=	ENSP00000507175.1:n.*475-71A=
ENST00000684254.1:c.*530-71A=	ENSP00000508001.1:n.*530-71A=
ENST00000684310.1:c.66-71A=	ENSP00000507550.1:n.66-71A=
ENST00000684530.1:c.66-71A=	ENSP00000507439.1:n.66-71A=
ENST00000684652.1:n.1735A=
ENST00000340941.11:c.804-71A= MANE Select	ENSP00000343657.6:n.804-71A=
ENST00000340941.10:c.804-71A=	ENSP00000343657.6:n.804-71A=
ENST00000505435.3:n.155-71A=
ENST00000505787.7:n.618-71A=
ENST00000509358.6:c.804-71A=	ENSP00000420994.2:n.804-71A=
ENST00000509539.2:c.129-71A=	ENSP00000425474.2:n.129-71A=
ENST00000510895.6:n.418-71A=
ENST00000512218.6:c.690-71A=	ENSP00000423202.2:n.690-71A=
ENST00000629193.2:c.690-71A=	ENSP00000486535.1:n.690-71A=
NM_022132.4:c.804-71A=	NP_071415.1:n.804-71A=
XM_005248567.1:c.690-71A=	XP_005248624.1:n.690-71A=
XM_011543528.1:c.804-71A=	XP_011541830.1:n.804-71A=
XM_011543529.1:c.804-71A=	XP_011541831.1:n.804-71A=
NM_001363147.1:c.690-71A=	NP_001350076.1:n.690-71A=
XM_011543529.2:c.804-71A=	XP_011541831.1:n.804-71A=
XM_017009688.1:c.804-71A=	XP_016865177.1:n.804-71A=
XR_001742172.1:n.844-71A=
NM_022132.5:c.804-71A= MANE Select	NP_071415.1:n.804-71A=