Canonical Allele Identifier: CA2838512076

Gene: CCDC38 SNRPF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95872518C>A , CM000674.2:g.95872518C>A	GRCh38
NC_000012.11:g.96266296C>A , CM000674.1:g.96266296C>A	GRCh37
NC_000012.10:g.94790427C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344280.8:c.1279-58G>T (CCDC38) MANE Select	ENSP00000345470.3:n.1279-58G>T
ENST00000344280.7:c.1279-58G>T (CCDC38)	ENSP00000345470.3:n.1279-58G>T
ENST00000549876.5:c.165-58G>T (CCDC38)
ENST00000552085.1:c.130-7170C>A (SNRPF)	ENSP00000447127.1:n.130-7170C>A
ENST00000553192.5:c.130-7170C>A (SNRPF)	ENSP00000447751.1:n.130-7170C>A
NM_182496.2:c.1279-58G>T (CCDC38)	NP_872302.2:n.1279-58G>T
XM_006719229.1:c.787-58G>T (CCDC38)	XP_006719292.1:n.787-58G>T
XM_011537883.1:c.1279-58G>T (CCDC38)	XP_011536185.1:n.1279-58G>T
XM_011537884.1:c.1159-58G>T (CCDC38)	XP_011536186.1:n.1159-58G>T
XM_011537885.1:c.1159-58G>T (CCDC38)	XP_011536187.1:n.1159-58G>T
XM_011537886.1:c.1159-58G>T (CCDC38)	XP_011536188.1:n.1159-58G>T
XM_011537887.1:c.1159-58G>T (CCDC38)	XP_011536189.1:n.1159-58G>T
XM_011537888.1:c.628-58G>T (CCDC38)	XP_011536190.1:n.628-58G>T
XR_429080.1:n.1511-58G>T (CCDC38)
XM_006719229.2:c.787-58G>T (CCDC38)	XP_006719292.1:n.787-58G>T
XM_011537883.2:c.1279-58G>T (CCDC38)	XP_011536185.1:n.1279-58G>T
XM_011537884.2:c.1159-58G>T (CCDC38)	XP_011536186.1:n.1159-58G>T
XM_011537886.2:c.1159-58G>T (CCDC38)	XP_011536188.1:n.1159-58G>T
XM_011537887.2:c.1159-58G>T (CCDC38)	XP_011536189.1:n.1159-58G>T
XM_011537888.3:c.628-58G>T (CCDC38)	XP_011536190.1:n.628-58G>T
NM_182496.3:c.1279-58G>T (CCDC38) MANE Select	NP_872302.2:n.1279-58G>T