Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77278689C>T , CM000676.2:g.77278689C>T	GRCh38
NC_000014.8:g.77745032C>T , CM000676.1:g.77745032C>T	GRCh37
NC_000014.7:g.76814785C>T	NCBI36
NG_008897.1:g.47194G>A , LRG_844:g.47194G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555134.2:n.957+40G>A
ENST00000556394.2:c.1573+40G>A	ENSP00000451967.2:n.1573+40G>A
ENST00000682247.1:c.2021+40G>A	ENSP00000507213.1:n.2021+40G>A
ENST00000682395.1:n.2496+40G>A
ENST00000682459.1:n.1735+40G>A
ENST00000682467.1:c.1892-181G>A	ENSP00000508062.1:n.1892-181G>A
ENST00000682795.1:c.2179+40G>A	ENSP00000507574.1:n.2179+40G>A
ENST00000682895.1:n.1748+40G>A
ENST00000682955.1:n.1606+40G>A
ENST00000683188.1:c.2293+40G>A
ENST00000683380.1:n.1696+40G>A
ENST00000683907.1:c.297+40G>A	ENSP00000507754.1:n.297+40G>A
ENST00000684259.1:n.3799+40G>A
ENST00000684538.1:n.1411+40G>A
ENST00000684549.1:n.1583+40G>A
ENST00000261534.9:c.2032+40G>A MANE Select	ENSP00000261534.4:n.2032+40G>A
ENST00000261534.8:c.2032+40G>A	ENSP00000261534.4:n.2032+40G>A
ENST00000452340.7:n.3008+40G>A
ENST00000554767.5:n.2818+40G>A
ENST00000555710.1:c.393+40G>A	ENSP00000451730.1:n.393+40G>A
ENST00000556394.1:c.88-181G>A
ENST00000556446.1:n.333+40G>A
ENST00000602717.5:c.247+40G>A	ENSP00000487704.1:n.247+40G>A
NM_013382.5:c.2032+40G>A , LRG_844t1:c.2032+40G>A	NP_037514.2:n.2032+40G>A
XM_011536675.1:c.2221+40G>A	XP_011534977.1:n.2221+40G>A
XM_011536676.1:c.1888+40G>A	XP_011534978.1:n.1888+40G>A
XM_011536677.1:c.1762+40G>A	XP_011534979.1:n.1762+40G>A
XM_011536679.1:c.1315+40G>A	XP_011534981.1:n.1315+40G>A
XR_943416.1:n.2285+40G>A
XM_011536675.2:c.2221+40G>A	XP_011534977.1:n.2221+40G>A
XM_011536676.2:c.1888+40G>A	XP_011534978.1:n.1888+40G>A
XM_011536677.3:c.1762+40G>A	XP_011534979.1:n.1762+40G>A
XR_001750279.1:n.2318+40G>A
XR_001750282.1:n.2971+40G>A
XR_943416.3:n.2283+40G>A
NM_013382.6:c.2032+40G>A	NP_037514.2:n.2032+40G>A
NM_013382.7:c.2032+40G>A MANE Select	NP_037514.2:n.2032+40G>A

Linked Data

Genomic Alleles

Transcript Alleles