Canonical Allele Identifier: CA245498849

Gene: ADGRD1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131091646C>T , CM000674.2:g.131091646C>T	GRCh38
NC_000012.11:g.131576191C>T , CM000674.1:g.131576191C>T	GRCh37
NC_000012.10:g.130142144C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261654.10:c.1671+6983C>T MANE Select	ENSP00000261654.5:n.1671+6983C>T
ENST00000261654.9:c.1671+6983C>T	ENSP00000261654.5:n.1671+6983C>T
ENST00000335486.10:c.21+6983C>T	ENSP00000334127.7:n.21+6983C>T
ENST00000376682.8:n.984+6983C>T
ENST00000446583.6:c.21+6983C>T	ENSP00000482235.1:n.21+6983C>T
ENST00000535015.5:c.1767+6983C>T	ENSP00000444425.1:n.1767+6983C>T
ENST00000543617.2:c.228+6983C>T	ENSP00000438021.1:n.228+6983C>T
NM_198827.3:c.1671+6983C>T	NP_942122.2:n.1671+6983C>T
XM_005253566.1:c.1491+6983C>T	XP_005253623.1:n.1491+6983C>T
XM_011538203.1:c.1767+6983C>T	XP_011536505.1:n.1767+6983C>T
XM_011538204.1:c.1767+6983C>T	XP_011536506.1:n.1767+6983C>T
XM_011538205.1:c.1587+6983C>T	XP_011536507.1:n.1587+6983C>T
XM_011538206.1:c.1767+6983C>T	XP_011536508.1:n.1767+6983C>T
XM_011538207.1:c.1767+6983C>T	XP_011536509.1:n.1767+6983C>T
XM_011538208.1:c.1332+6983C>T	XP_011536510.1:n.1332+6983C>T
XM_011538209.1:c.1767+6983C>T	XP_011536511.1:n.1767+6983C>T
XM_011538211.1:c.759+6983C>T	XP_011536513.1:n.759+6983C>T
XM_011538212.1:c.537+6983C>T	XP_011536514.1:n.537+6983C>T
NM_001330497.1:c.1767+6983C>T	NP_001317426.1:n.1767+6983C>T
NM_198827.4:c.1671+6983C>T	NP_942122.2:n.1671+6983C>T
XM_005253566.2:c.1491+6983C>T	XP_005253623.1:n.1491+6983C>T
XM_011538204.2:c.1767+6983C>T	XP_011536506.1:n.1767+6983C>T
XM_011538205.2:c.1587+6983C>T	XP_011536507.1:n.1587+6983C>T
XM_011538206.2:c.1767+6983C>T	XP_011536508.1:n.1767+6983C>T
XM_011538207.2:c.1767+6983C>T	XP_011536509.1:n.1767+6983C>T
XM_011538208.2:c.1332+6983C>T	XP_011536510.1:n.1332+6983C>T
XM_011538209.2:c.1767+6983C>T	XP_011536511.1:n.1767+6983C>T
XM_011538211.2:c.759+6983C>T	XP_011536513.1:n.759+6983C>T
XM_011538212.2:c.537+6983C>T	XP_011536514.1:n.537+6983C>T
NM_198827.5:c.1671+6983C>T MANE Select	NP_942122.2:n.1671+6983C>T
NM_001330497.2:c.1767+6983C>T	NP_001317426.1:n.1767+6983C>T