Canonical Allele Identifier: CA1476187638

Gene: CCSER1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.91494378G= , CM000666.2:g.91494378G=	GRCh38
NC_000004.11:g.92415529G= , CM000666.1:g.92415529G=	GRCh37
NC_000004.10:g.92634552G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509176.6:c.2218-104194G= MANE Select	ENSP00000425040.1:n.2218-104194G=
ENST00000649522.1:c.92-104194G=	ENSP00000497818.1:n.92-104194G=
ENST00000509176.5:c.2218-104194G=	ENSP00000425040.1:n.2218-104194G=
NM_001145065.1:c.2218-104194G=	NP_001138537.1:n.2218-104194G=
XM_011531936.1:c.2314-104194G=	XP_011530238.1:n.2314-104194G=
XM_011531937.1:c.2314-104194G=	XP_011530239.1:n.2314-104194G=
XM_011531938.1:c.2314-104194G=	XP_011530240.1:n.2314-104194G=
XM_011531939.1:c.2314-104194G=	XP_011530241.1:n.2314-104194G=
XM_011531940.1:c.2236-104194G=	XP_011530242.1:n.2236-104194G=
XM_011531937.2:c.2314-104194G=	XP_011530239.1:n.2314-104194G=
XM_011531938.2:c.2314-104194G=	XP_011530240.1:n.2314-104194G=
XM_011531939.2:c.2314-104194G=	XP_011530241.1:n.2314-104194G=
XM_017008194.1:c.2314-104194G=	XP_016863683.1:n.2314-104194G=
NM_001145065.2:c.2218-104194G= MANE Select	NP_001138537.1:n.2218-104194G=