Canonical Allele Identifier: CA14401349

Gene: CSF3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40017649C>T , CM000679.2:g.40017649C>T	GRCh38
NC_000017.10:g.38173902C>T , CM000679.1:g.38173902C>T	GRCh37
NC_000017.9:g.35427428C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394149.8:c.*690C>T MANE Select	ENSP00000377705.4:n.*690C>T
ENST00000225474.6:c.*690C>T	ENSP00000225474.2:n.*690C>T
ENST00000331769.6:c.*690C>T	ENSP00000327766.2:n.*690C>T
ENST00000394149.7:c.*690C>T	ENSP00000377705.3:n.*690C>T
ENST00000579852.1:c.*976C>T	ENSP00000464157.1:n.*976C>T
NM_000759.3:c.*690C>T	NP_000750.1:n.*690C>T
NM_001178147.1:c.*690C>T	NP_001171618.1:n.*690C>T
NM_172219.2:c.*690C>T	NP_757373.1:n.*690C>T
NM_172220.2:c.*690C>T	NP_757374.2:n.*690C>T
NR_033662.1:n.1595C>T
NM_000759.4:c.*690C>T	NP_000750.1:n.*690C>T
NM_001178147.2:c.*690C>T	NP_001171618.1:n.*690C>T
NM_172219.3:c.*690C>T MANE Select	NP_757373.1:n.*690C>T
NM_172220.3:c.*690C>T	NP_757374.2:n.*690C>T
NR_033662.2:n.1516C>T
NR_168489.1:n.1408C>T
NR_168490.1:n.1417C>T
NR_168491.1:n.1525C>T