Canonical Allele Identifier: CA366889683

Gene: AGR2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.16801149A>G , CM000669.2:g.16801149A>G	GRCh38
NC_000007.13:g.16840773A>G , CM000669.1:g.16840773A>G	GRCh37
NC_000007.12:g.16807298A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006408.4:c.256+2T>C MANE Select	NP_006399.1:n.256+2T>C
ENST00000419304.7:c.256+2T>C MANE Select	ENSP00000391490.2:n.256+2T>C
NM_006408.3:c.256+2T>C	NP_006399.1:n.256+2T>C
ENST00000401412.5:c.256+2T>C	ENSP00000386025.1:n.256+2T>C
ENST00000412973.1:c.256+2T>C	ENSP00000411969.1:n.256+2T>C
ENST00000419304.6:c.256+2T>C	ENSP00000391490.2:n.256+2T>C
ENST00000450569.5:c.46+2T>C	ENSP00000414806.1:n.46+2T>C
ENST00000489523.5:n.328+2T>C
XM_005249581.3:c.256+2T>C	XP_005249638.1:n.256+2T>C
XM_005249581.5:c.256+2T>C	XP_005249638.1:n.256+2T>C