Canonical Allele Identifier: CA1608613684

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585223_7585224delinsAG , CM000668.2:g.7585223_7585224delinsAG	GRCh38
NC_000006.11:g.7585456_7585457delinsAG , CM000668.1:g.7585456_7585457delinsAG	GRCh37
NC_000006.10:g.7530455_7530456delinsAG	NCBI36
NG_008803.1:g.48587_48588delinsAG , LRG_423:g.48587_48588delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6632_6633delinsAG	ENSP00000518230.1:p.Gln2211=
ENST00000379802.8:c.7961_7962delinsAG MANE Select	ENSP00000369129.3:p.Gln2654=
ENST00000379802.7:c.7961_7962delinsAG	ENSP00000369129.3:p.Gln2654=
ENST00000418664.2:c.6164_6165delinsAG	ENSP00000396591.2:p.Gln2055=
NM_001008844.1:c.6164_6165delinsAG	NP_001008844.1:p.Gln2055=
NM_004415.2:c.7961_7962delinsAG , LRG_423t1:c.7961_7962delinsAG	NP_004406.2:p.Gln2654=
XM_011514323.1:c.6632_6633delinsAG	XP_011512625.1:p.Gln2211=
NM_001008844.2:c.6164_6165delinsAG	NP_001008844.1:p.Gln2055=
NM_001319034.1:c.6632_6633delinsAG	NP_001305963.1:p.Gln2211=
NM_004415.3:c.7961_7962delinsAG	NP_004406.2:p.Gln2654=
NM_004415.4:c.7961_7962delinsAG MANE Select	NP_004406.2:p.Gln2654=
NM_001008844.3:c.6164_6165delinsAG	NP_001008844.1:p.Gln2055=
NM_001319034.2:c.6632_6633delinsAG	NP_001305963.1:p.Gln2211=