Canonical Allele Identifier: CA491214611

Gene: EDC3

Linked Data

• MyVariant Identifiers: chr15:g.74967316T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74674975T>A , CM000677.2:g.74674975T>A	GRCh38
NC_000015.9:g.74967316T>A , CM000677.1:g.74967316T>A	GRCh37
NC_000015.8:g.72754369T>A	NCBI36
NG_054910.1:g.26071A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000315127.9:c.150A>T MANE Select	ENSP00000320503.4:p.Pro50=
ENST00000647659.1:c.150A>T	ENSP00000497737.1:p.Pro50=
ENST00000315127.8:c.150A>T	ENSP00000320503.4:p.Pro50=
ENST00000426797.7:c.150A>T	ENSP00000401343.3:p.Pro50=
ENST00000563009.5:c.150A>T	ENSP00000455503.1:p.Pro50=
ENST00000563292.1:c.150A>T	ENSP00000454317.1:p.Pro50=
ENST00000565602.5:c.150A>T	ENSP00000454885.1:p.Pro50=
ENST00000566219.1:c.-65-18907A>T	ENSP00000456805.1:n.-65-18907A>T
ENST00000566243.5:c.150A>T	ENSP00000457523.1:p.Pro50=
ENST00000566828.5:c.150A>T	ENSP00000455870.1:p.Pro50=
ENST00000567813.1:c.150A>T	ENSP00000457156.1:p.Pro50=
ENST00000568176.5:c.150A>T	ENSP00000455580.1:p.Pro50=
ENST00000569007.1:n.265A>T
ENST00000569561.5:c.150A>T	ENSP00000455589.1:p.Pro50=
ENST00000570138.5:c.150A>T	ENSP00000457170.1:p.Pro50=
NM_001142443.1:c.150A>T	NP_001135915.1:p.Pro50=
NM_001142444.1:c.150A>T	NP_001135916.1:p.Pro50=
NM_025083.3:c.150A>T	NP_079359.2:p.Pro50=
XM_011522091.1:c.150A>T	XP_011520393.1:p.Pro50=
NM_001142443.2:c.150A>T	NP_001135915.1:p.Pro50=
NM_001142444.2:c.150A>T	NP_001135916.1:p.Pro50=
NM_001351378.1:c.150A>T	NP_001338307.1:p.Pro50=
NM_001351379.1:c.-281A>T	NP_001338308.1:n.-281A>T
NM_025083.4:c.150A>T	NP_079359.2:p.Pro50=
XM_024450077.1:c.150A>T	XP_024305845.1:p.Pro50=
XM_024450078.1:c.150A>T	XP_024305846.1:p.Pro50=
XM_024450079.1:c.150A>T	XP_024305847.1:p.Pro50=
NM_025083.5:c.150A>T MANE Select	NP_079359.2:p.Pro50=
NM_001142443.3:c.150A>T	NP_001135915.1:p.Pro50=
NM_001142444.3:c.150A>T	NP_001135916.1:p.Pro50=
NM_001351378.2:c.150A>T	NP_001338307.1:p.Pro50=
NM_001351379.2:c.-281A>T	NP_001338308.1:n.-281A>T