Canonical Allele Identifier: CA11054996

Gene: ALLC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3701381T>C , CM000664.2:g.3701381T>C	GRCh38
NC_000002.11:g.3748971T>C , CM000664.1:g.3748971T>C	GRCh37
NC_000002.10:g.3726846T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252505.4:c.851-131T>C MANE Select	ENSP00000252505.3:n.851-131T>C
ENST00000252505.3:c.851-131T>C	ENSP00000252505.3:n.851-131T>C
ENST00000471711.1:n.515-131T>C
ENST00000476389.5:n.1436-131T>C
NM_018436.3:c.851-131T>C	NP_060906.3:n.851-131T>C
XM_005263851.2:c.386-131T>C	XP_005263908.2:n.386-131T>C
XM_011510369.1:c.716-131T>C	XP_011508671.1:n.716-131T>C
XM_011510370.1:c.440-131T>C	XP_011508672.1:n.440-131T>C
XM_011510371.1:c.440-131T>C	XP_011508673.1:n.440-131T>C
XR_922731.1:n.349+1427A>G
XR_922733.1:n.385+1427A>G
XM_011510369.2:c.716-131T>C	XP_011508671.1:n.716-131T>C
XM_011510370.2:c.440-131T>C	XP_011508672.1:n.440-131T>C
XM_017004495.1:c.1055-131T>C	XP_016859984.1:n.1055-131T>C
XM_017004496.2:c.716-131T>C	XP_016859985.1:n.716-131T>C
XM_017004497.1:c.440-131T>C	XP_016859986.1:n.440-131T>C
XM_017004498.1:c.386-131T>C	XP_016859987.1:n.386-131T>C
NM_018436.4:c.851-131T>C MANE Select	NP_060906.3:n.851-131T>C