Canonical Allele Identifier: CA1554387611

Gene: MCCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71634758T= , CM000667.2:g.71634758T=	GRCh38
NC_000005.9:g.70930585T= , CM000667.1:g.70930585T=	GRCh37
NC_000005.8:g.70966341T=	NCBI36
NG_008882.1:g.52471T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.760-185T=
ENST00000505787.8:n.2644-185T=
ENST00000509358.7:c.804-185T=	ENSP00000420994.3:n.804-185T=
ENST00000509539.3:c.66-185T=	ENSP00000425474.3:n.66-185T=
ENST00000510895.7:n.927-185T=
ENST00000629193.3:c.690-185T=	ENSP00000486535.2:n.690-185T=
ENST00000681968.1:c.297-185T=	ENSP00000508143.1:n.297-185T=
ENST00000682045.1:c.660-185T=	ENSP00000507329.1:n.660-185T=
ENST00000682214.1:c.411-185T=	ENSP00000507336.1:n.411-185T=
ENST00000682499.1:n.1625-185T=
ENST00000682541.1:c.804-185T=	ENSP00000507673.1:n.804-185T=
ENST00000682687.1:c.804-185T=	ENSP00000507945.1:n.804-185T=
ENST00000682727.1:c.804-185T=	ENSP00000507393.1:n.804-185T=
ENST00000682876.1:c.933-185T=	ENSP00000508389.1:n.933-185T=
ENST00000683098.1:c.803+2573T=	ENSP00000507670.1:n.803+2573T=
ENST00000683258.1:c.*525-185T=	ENSP00000507448.1:n.*525-185T=
ENST00000683339.1:c.588-185T=	ENSP00000507758.1:n.588-185T=
ENST00000683403.1:c.804-185T=	ENSP00000507896.1:n.804-185T=
ENST00000683429.1:c.411-185T=	ENSP00000507697.1:n.411-185T=
ENST00000683665.1:c.804-185T=	ENSP00000507068.1:n.804-185T=
ENST00000683789.1:c.690-185T=	ENSP00000507012.1:n.690-185T=
ENST00000683847.1:n.648-185T=
ENST00000683882.1:c.804-185T=	ENSP00000506735.1:n.804-185T=
ENST00000684024.1:c.*475-185T=	ENSP00000507175.1:n.*475-185T=
ENST00000684254.1:c.*530-185T=	ENSP00000508001.1:n.*530-185T=
ENST00000684310.1:c.66-185T=	ENSP00000507550.1:n.66-185T=
ENST00000684530.1:c.66-185T=	ENSP00000507439.1:n.66-185T=
ENST00000684652.1:n.1621T=
ENST00000340941.11:c.804-185T= MANE Select	ENSP00000343657.6:n.804-185T=
ENST00000340941.10:c.804-185T=	ENSP00000343657.6:n.804-185T=
ENST00000505435.3:n.155-185T=
ENST00000505787.7:n.618-185T=
ENST00000509358.6:c.804-185T=	ENSP00000420994.2:n.804-185T=
ENST00000509539.2:c.129-185T=	ENSP00000425474.2:n.129-185T=
ENST00000510895.6:n.418-185T=
ENST00000512218.6:c.690-185T=	ENSP00000423202.2:n.690-185T=
ENST00000629193.2:c.690-185T=	ENSP00000486535.1:n.690-185T=
NM_022132.4:c.804-185T=	NP_071415.1:n.804-185T=
XM_005248567.1:c.690-185T=	XP_005248624.1:n.690-185T=
XM_011543528.1:c.804-185T=	XP_011541830.1:n.804-185T=
XM_011543529.1:c.804-185T=	XP_011541831.1:n.804-185T=
NM_001363147.1:c.690-185T=	NP_001350076.1:n.690-185T=
XM_011543529.2:c.804-185T=	XP_011541831.1:n.804-185T=
XM_017009688.1:c.804-185T=	XP_016865177.1:n.804-185T=
XR_001742172.1:n.844-185T=
NM_022132.5:c.804-185T= MANE Select	NP_071415.1:n.804-185T=